3177 lines
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Entry
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- #620536 - ALPORT SYNDROME 3B, AUTOSOMAL RECESSIVE; ATS3B
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- OMIM
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<p>
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<span class="h4">#620536</span>
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<br />
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<strong>Table of Contents</strong>
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<a href="#title"><strong>Title</strong></a>
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<a href="#phenotypeMap"><strong>Phenotype-Gene Relationships</strong></a>
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<li role="presentation">
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<a href="/clinicalSynopsis/620536"><strong>Clinical Synopsis</strong></a>
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<a href="/phenotypicSeries/PS301050"> <strong>Phenotypic Series</strong> </a>
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<a href="#text"><strong>Text</strong></a>
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<a href="#description">Description</a>
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<a href="#clinicalFeatures">Clinical Features</a>
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<a href="#inheritance">Inheritance</a>
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<a href="#molecularGenetics">Molecular Genetics</a>
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<a href="#clinicalManagement">Clinical Management</a>
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<li role="presentation" style="margin-left: 1em">
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<a href="#pathogenesis">Pathogenesis</a>
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<a href="#populationGenetics">Population Genetics</a>
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<a href="#seeAlso"><strong>See Also</strong></a>
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<li role="presentation">
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<a href="#references"><strong>References</strong></a>
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<li role="presentation">
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<a href="#contributors"><strong>Contributors</strong></a>
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<a href="#creationDate"><strong>Creation Date</strong></a>
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<li role="presentation">
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<a href="#editHistory"><strong>Edit History</strong></a>
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<a href="#mimExternalLinksFold" id="mimExternalLinksToggle" class="mimTriangleToggle" role="button" data-toggle="collapse">
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<div style="display: table-row">
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<div id="mimExternalLinksToggleTriangle" class="small" style="color: white; display: table-cell;">▼</div>
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<div style="display: table-cell;">External Links</div>
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</div>
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</a>
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</h4>
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<div class="panel-heading mim-panel-heading" role="tab" id="mimClinicalResources">
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<span class="panel-title">
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<span class="small">
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<a href="#mimClinicalResourcesLinksFold" id="mimClinicalResourcesLinksToggle" class=" mimSingletonTriangleToggle" role="button" data-toggle="collapse" data-parent="#mimExternalLinksAccordion">
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<div style="display: table-row">
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<div id="mimClinicalResourcesLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5; display: table-cell;">▼</div>
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<div style="display: table-cell;">Clinical Resources</div>
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</div>
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</a>
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</span>
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</span>
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<div class="panel-body small mim-panel-body">
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<div><a href="https://clinicaltrials.gov/search?cond=ALPORT SYNDROME 3B, AUTOSOMAL RECESSIVE" class="mim-tip-hint" title="A registry of federally and privately supported clinical trials conducted in the United States and around the world." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></div>
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<div><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=11851&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></div>
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<div><a href="https://www.ncbi.nlm.nih.gov/books/NBK1207/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></div>
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<div><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=620536[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></div>
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<div><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=88919" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></div>
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<span>
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<span class="mim-tip-bottom" qtip_title="<strong>Looking for this gene or this phenotype in other resources?</strong>" qtip_text="Select a related resource from the dropdown menu and click for a targeted link to information directly relevant.">
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</span>
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</span>
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<div>
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<a id="title" class="mim-anchor"></a>
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<div>
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<a id="number" class="mim-anchor"></a>
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<div class="text-right">
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<a href="#" class="mim-tip-icd" qtip_title="<strong>ICD+</strong>" qtip_text="
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<strong>ORPHA:</strong> 88919<br />
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">ICD+</a>
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</div>
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<div>
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<span class="h3">
|
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<span class="mim-font mim-tip-hint" title="Phenotype description, molecular basis known">
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<span class="text-danger"><strong>#</strong></span>
|
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620536
|
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</span>
|
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</span>
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</div>
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</div>
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<div>
|
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<a id="preferredTitle" class="mim-anchor"></a>
|
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<h3>
|
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<span class="mim-font">
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ALPORT SYNDROME 3B, AUTOSOMAL RECESSIVE; ATS3B
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</span>
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</h3>
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</div>
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<div>
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<br />
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</div>
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</div>
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<div>
|
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<a id="phenotypeMap" class="mim-anchor"></a>
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<h4>
|
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<span class="mim-font">
|
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<strong>Phenotype-Gene Relationships</strong>
|
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</span>
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</h4>
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<div>
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<table class="table table-bordered table-condensed table-hover small mim-table-padding">
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<thead>
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<tr class="active">
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<th>
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Location
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</th>
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<th>
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Phenotype
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</th>
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<th>
|
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Phenotype <br /> MIM number
|
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</th>
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<th>
|
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Inheritance
|
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</th>
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<th>
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Phenotype <br /> mapping key
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</th>
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<th>
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Gene/Locus
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</th>
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<th>
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Gene/Locus <br /> MIM number
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<tbody>
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<tr>
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<td>
|
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<span class="mim-font">
|
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<a href="/geneMap/2/1071?start=-3&limit=10&highlight=1071">
|
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2q36.3
|
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</a>
|
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</span>
|
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</td>
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<td>
|
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<span class="mim-font">
|
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Alport syndrome 3B, autosomal recessive
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</span>
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</td>
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<td>
|
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<span class="mim-font">
|
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<a href="/entry/620536"> 620536 </a>
|
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</span>
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</td>
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<td>
|
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<span class="mim-font">
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<abbr class="mim-tip-hint" title="Autosomal recessive">AR</abbr>
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</span>
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</td>
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<td>
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<span class="mim-font">
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<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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</span>
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</td>
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<td>
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<span class="mim-font">
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COL4A3
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</span>
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</td>
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<td>
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<span class="mim-font">
|
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<a href="/entry/120070"> 120070 </a>
|
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</span>
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</td>
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</tr>
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</tbody>
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</table>
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<div>
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<div class="btn-group mim-changed mim-change">
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<a href="/clinicalSynopsis/620536" class="btn btn-warning" role="button"> Clinical Synopsis </a>
|
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<button type="button" id="mimPhenotypicSeriesToggle" class="btn btn-warning dropdown-toggle mimSingletonFoldToggle" data-toggle="collapse" href="#mimClinicalSynopsisFold" onclick="ga('send', 'event', 'Unfurl', 'ClinicalSynopsis', 'omim.org')">
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<span class="caret"></span>
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<span class="sr-only">Toggle Dropdown</span>
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</button>
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</div>
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<div class="btn-group">
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<a href="/phenotypicSeries/PS301050" class="btn btn-info" role="button"> Phenotypic Series </a>
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<button type="button" id="mimPhenotypicSeriesToggle" class="btn btn-info dropdown-toggle mimSingletonFoldToggle" data-toggle="collapse" href="#mimPhenotypicSeriesFold" onclick="ga('send', 'event', 'Unfurl', 'PhenotypicSeries', 'omim.org')">
|
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<span class="caret"></span>
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<span class="sr-only">Toggle Dropdown</span>
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</button>
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<div class="btn-group">
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<button type="button" class="btn btn-success dropdown-toggle" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false">
|
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PheneGene Graphics <span class="caret"></span>
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</button>
|
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<ul class="dropdown-menu" style="width: 17em;">
|
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<li><a href="/graph/linear/620536" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Linear'})"> Linear </a></li>
|
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<li><a href="/graph/radial/620536" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Radial'})"> Radial </a></li>
|
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</ul>
|
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</div>
|
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<span class="glyphicon glyphicon-question-sign mim-tip-hint" title="OMIM PheneGene graphics depict relationships between phenotypes, groups of related phenotypes (Phenotypic Series), and genes.<br /><a href='/static/omim/pdf/OMIM_Graphics.pdf' target='_blank'>A quick reference overview and guide (PDF)</a>"></span>
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<p />
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</div>
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<div id="mimClinicalSynopsisFold" class="well well-sm collapse mimSingletonToggleFold">
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<div class="small" style="margin: 5px">
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<div>
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<div>
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<span class="h5 mim-font">
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<strong> INHERITANCE </strong>
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</span>
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</div>
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<div style="margin-left: 2em;">
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<div>
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<span class="mim-font">
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<div class="mim-changed mim-change"> - Autosomal recessive <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/258211005" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">258211005</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0441748&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0441748</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000007" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000007</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000007" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000007</a>]</span><br /></div>
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</span>
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</div>
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</div>
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</div>
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<div>
|
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<div>
|
|
<span class="h5 mim-font">
|
|
<strong> HEAD & NECK </strong>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
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<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<em> Ears </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
<div class="mim-changed mim-change"> - Sensorineural hearing loss <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/60700002" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">60700002</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/H90.5" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">H90.5</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/389.10" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389.10</a>, <a href="https://purl.bioontology.org/ontology/ICD9CM/389.1" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389.1</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0018784&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0018784</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000407" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000407</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000407" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000407</a>]</span><br /></div>
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</span>
|
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</div>
|
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</div>
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</div>
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</div>
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<div>
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<div>
|
|
<span class="h5 mim-font">
|
|
<strong> GENITOURINARY </strong>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
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<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<em> Kidneys </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
<div class="mim-changed mim-change"> - Glomerulonephropathy <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/197679002" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">197679002</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/N00-N08" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N00-N08</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/N05" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N05</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0268731&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0268731</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0100820" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0100820</a>]</span><br /> -
|
|
End-stage renal failure <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/90688005" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">90688005</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/46177005" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">46177005</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/433146000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">433146000</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/N18.5" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N18.5</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/N18.9" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N18.9</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/N18.6" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N18.6</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/585.6" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">585.6</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0022661&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0022661</a>, <a href="https://bioportal.bioontology.org/search?q=C2316810&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C2316810</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003774" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003774</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003774" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003774</a>]</span><br /> -
|
|
Nephrotic syndrome <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/52254009" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">52254009</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/N04" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N04</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/581" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">581</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0027726&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0027726</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000100" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000100</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000100" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000100</a>]</span><br /> -
|
|
Lamellation and splitting of the glomerular basement membrane<br /></div>
|
|
|
|
</span>
|
|
</div>
|
|
</div>
|
|
|
|
|
|
|
|
</div>
|
|
|
|
</div>
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|
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|
|
<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<strong> LABORATORY ABNORMALITIES </strong>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
|
|
<div>
|
|
<span class="mim-font">
|
|
|
|
<div class="mim-changed mim-change"> - Hematuria (gross and microscopic) <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/53298000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">53298000</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/34436003" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">34436003</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/R31" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">R31</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/R31.9" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">R31.9</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/599.7" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">599.7</a>, <a href="https://purl.bioontology.org/ontology/ICD9CM/599.70" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">599.70</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0018965&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0018965</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000790" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000790</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000790" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000790</a>]</span><br /> -
|
|
Proteinuria <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/29738008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">29738008</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/231860006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">231860006</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/R80.9" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">R80.9</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/R80" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">R80</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/791.0" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">791.0</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1279888&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1279888</a>, <a href="https://bioportal.bioontology.org/search?q=C0033687&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0033687</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000093" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000093</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000093" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000093</a>]</span><br /></div>
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|
|
</span>
|
|
</div>
|
|
|
|
</div>
|
|
|
|
</div>
|
|
|
|
|
|
|
|
|
|
<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<strong> MISCELLANEOUS </strong>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
|
|
<div>
|
|
<span class="mim-font">
|
|
|
|
<div class="mim-changed mim-change"> - Microscopic hematuria in some heterozygous carriers (<a href="/entry/620320">620320</a>)<br /></div>
|
|
|
|
</span>
|
|
</div>
|
|
|
|
</div>
|
|
|
|
</div>
|
|
|
|
|
|
|
|
|
|
<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<strong> MOLECULAR BASIS </strong>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
|
|
<div>
|
|
<span class="mim-font">
|
|
|
|
<div class="mim-changed mim-change"> - Caused by mutation in the collagen IV, alpha-3 polypeptide gene (COL4A3, <a href="/entry/120070#0001">120070.0001</a>)<br /></div>
|
|
|
|
</span>
|
|
</div>
|
|
|
|
</div>
|
|
|
|
</div>
|
|
|
|
|
|
|
|
|
|
<div class="text-right">
|
|
<a href="#mimClinicalSynopsisFold" data-toggle="collapse">▲ Close</a>
|
|
</div>
|
|
</div>
|
|
</div>
|
|
|
|
|
|
|
|
|
|
|
|
<div id="mimPhenotypicSeriesFold" class="well well-sm collapse mimSingletonToggleFold">
|
|
<div class="small">
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
<div class="row">
|
|
<div class="col-lg-12 col-md-12 col-sm-12 col-xs-12">
|
|
<h5>
|
|
Alport syndrome
|
|
- <a href="/phenotypicSeries/PS301050">PS301050</a>
|
|
- 4 Entries
|
|
</h5>
|
|
</div>
|
|
</div>
|
|
|
|
<div class="row" style="margin-left: 0.125em; margin-right: 0.125em;">
|
|
<table class="table table-bordered table-condensed table-hover mim-table-padding">
|
|
<thead>
|
|
<tr>
|
|
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
|
|
<strong>Location</strong>
|
|
</th>
|
|
<th class="col-lg-5 col-md-5 col-sm-5 col-xs-6 text-nowrap">
|
|
<strong>Phenotype</strong>
|
|
</th>
|
|
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
|
|
<strong>Inheritance</strong>
|
|
</th>
|
|
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
|
|
<strong>Phenotype<br />mapping key</strong>
|
|
</th>
|
|
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
|
|
<strong>Phenotype<br />MIM number</strong>
|
|
</th>
|
|
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
|
|
<strong>Gene/Locus</strong>
|
|
</th>
|
|
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
|
|
<strong>Gene/Locus<br />MIM number</strong>
|
|
</th>
|
|
</tr>
|
|
</thead>
|
|
<tbody>
|
|
|
|
<tr>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<a href="/geneMap/2/1070?start=-3&limit=10&highlight=1070"> 2q36.3 </a>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/203780"> Alport syndrome 2, autosomal recessive </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</abbr>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/203780"> 203780 </a>
|
|
</span>
|
|
</td>
|
|
<td>
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<p>A number sign (#) is used with this entry because of evidence that autosomal recessive Alport syndrome-3B (ATS3B) is caused by homozygous or compound heterozygous mutation in the COL4A3 (<a href="/entry/120070">120070</a>) gene on chromosome 2q36.</p><p>Another form of autosomal recessive Alport syndrome (ATS2; <a href="/entry/120131">120131</a>) results from homozygous or compound heterozygous mutation in the COL4A4 gene (<a href="/entry/120131">120131</a>) on chromosome 2q36.</p>
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<p>Autosomal recessive Alport syndrome-3B (ATS3B) is a progressive hematuric glomerulonephritis characterized by glomerular basement membrane abnormalities. Sensorineural hearing loss and ocular manifestations may be present (summary by <a href="#1" class="mim-tip-reference" title="Boye, E., Mollet, G., Forestier, L., Cohen-Solal, L., Heidet, L., Cochat, P., Grunfeld, J.-P., Palcoux, J.-B., Gubler, M.-C., Antignac, C. <strong>Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.</strong> Am. J. Hum. Genet. 63: 1329-1340, 1998.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9792860/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9792860</a>] [<a href="https://doi.org/10.1086/302106" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9792860">Boye et al., 1998</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9792860" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>For a general phenotypic description of Alport syndrome, see the X-linked dominant form (ATS1; <a href="/entry/301050">301050</a>).</p>
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<p><a href="#16" class="mim-tip-reference" title="Passwell, J. H., David, R., Boichis, H., Herzfeld, S. <strong>Hereditary nephritis with associated defects in proximal renal tubular function.</strong> J. Pediat. 98: 85-87, 1981.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7452412/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7452412</a>] [<a href="https://doi.org/10.1016/s0022-3476(81)80545-8" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7452412">Passwell et al. (1981)</a> described a girl, born of first-cousin parents, who presented in the first year of life with failure to thrive and was found to have nephritis and deafness. She showed the characteristic electron microscopic feature of Alport syndrome, including thickening and splitting of the basement membranes of both the glomeruli and the tubules into thin layers, with accumulation of electron dense particles within this network. The parents were unaffected, but 2 maternal uncles had chronic nephritis and neurosensory deafness. An unusual feature was Fanconi syndrome in the proband. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7452412" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#15" class="mim-tip-reference" title="Mochizuki, T., Lemmink, H. H., Mariyama, M., Antignac, C., Gubler, M.-C., Pirson, Y., Verellen-Dumoulin, C., Chan, B., Schroder, C. H., Smeets, H. J., Reeders, S. T. <strong>Identification of mutations in the alpha-3(IV) and alpha-4(IV) collagen genes in autosomal recessive Alport syndrome.</strong> Nature Genet. 8: 77-81, 1994.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7987396/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7987396</a>] [<a href="https://doi.org/10.1038/ng0994-77" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7987396">Mochizuki et al. (1994)</a> reported 2 unrelated families with autosomal recessive Alport syndrome and mutation in the COL4A3 gene. In family VB, a brother and sister were affected. The girl developed hematuria at age 4 years and also had sensorineural deafness. She received a renal allograft at age 10 and developed antiglomerular basement membrane (GBM) nephritis 6 months later. Her brother had hematuria, deafness, and deteriorating renal function. The unaffected parents had no known consanguinity but originated from the same small village in the Netherlands. In consanguineous family DU, an 11-year-old Belgian girl developed proteinuria and microhematuria at age 7 years and end-stage renal disease at age 11 years. At age 11, she had renal transplant from her mother, and no rejection or anti-GBM nephritis had developed by age 16. At age 13, an audiogram showed bilateral sensorineural hearing loss. Both parents were unaffected and had normal renal function and urinalysis. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7987396" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#10" class="mim-tip-reference" title="Knebelmann, B., Forestier, L., Drouot, L., Quinones, S., Chuet, C., Benessy, F., Saus, J., Antignac, C. <strong>Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome.</strong> Hum. Molec. Genet. 4: 675-679, 1995.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7633417/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7633417</a>] [<a href="https://doi.org/10.1093/hmg/4.4.675" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7633417">Knebelmann et al. (1995)</a> studied a family (HO) from Reunion Island with autosomal recessive Alport syndrome and mutation in the COL4A3 gene. A brother and sister reached end-stage renal failure at 14 and 15 years of age, respectively. Both had sensorineural hearing loss requiring hearing aids; no ocular symptoms were found. The father and 2 brothers were asymptomatic, but the mother had intermittent microscopic hematuria. <a href="#4" class="mim-tip-reference" title="Finielz, P., Cartault, F., Chuet, C., Genin, R. <strong>Alport syndrome in Reunion Island: phenotypic heterogeneity of the recessive-autosomal form. (Letter)</strong> Nephron 79: 237 only, 1998.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9647515/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9647515</a>] [<a href="https://doi.org/10.1159/000045039" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9647515">Finielz et al. (1998)</a> identified the same mutation in 4 other families from Reunion Island. In 1 family, 3 individuals, all male, were involved. Two were placed on hemodialysis for end-stage renal disease at ages 28 and 26 years; the third, aged 13 years, had normal serum creatinine concentration values. The 3 other families, who were from a different town, had discovery of Alport syndrome at earlier ages ranging from 3 to 13 years on the basis of macroscopic hematuria and/or proteinuria, and in only 1 case was deafness evident. Males and females seemed to be equally involved (3 boys, 3 girls). End-stage renal failure occurred earlier (ages 14, 14, 18, and 15), unrelated to sex. Auditory impairment was a constant feature when evaluated; ocular impairment involved 1 patient only. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=9647515+7633417" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#2" class="mim-tip-reference" title="Colville, D., Savige, J., Morfis, M., Ellis, J., Kerr, P., Agar, J., Fasset, R. <strong>Ocular manifestations of autosomal recessive Alport syndrome.</strong> Ophthal. Genet. 18: 119-128, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9361309/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9361309</a>] [<a href="https://doi.org/10.3109/13816819709057125" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9361309">Colville et al. (1997)</a> examined the eyes of a family with autosomal recessive Alport syndrome. Four of the 8 offspring of a consanguineous marriage had renal failure and deafness by the age of 20 years. Studies of linkage to the COL4A5 (<a href="/entry/303630">303630</a>)/COL4A6 (<a href="/entry/303631">303631</a>) locus yielded strongly negative lod scores (excluding the X-linked form), whereas linkage to an intragenic marker for the COL4A3/COL4A4 locus showed positive lod scores consistent with the autosomal recessive form. All 4 affected members had anterior lenticonus, and the 3 who were examined had a dot-and-fleck retinopathy. <a href="#2" class="mim-tip-reference" title="Colville, D., Savige, J., Morfis, M., Ellis, J., Kerr, P., Agar, J., Fasset, R. <strong>Ocular manifestations of autosomal recessive Alport syndrome.</strong> Ophthal. Genet. 18: 119-128, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9361309/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9361309</a>] [<a href="https://doi.org/10.3109/13816819709057125" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9361309">Colville et al. (1997)</a> concluded that the ocular manifestations of autosomal recessive Alport syndrome are identical to those of the X-linked form. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9361309" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>To assess the prevalence of recurrent corneal erosion (RCE) in Alport syndrome, <a href="#17" class="mim-tip-reference" title="Rhys, C., Snyers, B., Pirson, Y. <strong>Recurrent corneal erosion associated with Alport's syndrome.</strong> Kidney Int. 52: 208-211, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9211364/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9211364</a>] [<a href="https://doi.org/10.1038/ki.1997.321" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9211364">Rhys et al. (1997)</a> surveyed 41 patients with Alport syndrome and renal failure and 67 control patients transplanted for another form of nephropathy. A history of RCE, first manifested between the ages of 12 and 21 years, was obtained in 7 Alport syndrome patients, 1 with probable autosomal recessive inheritance, but in only 1 control patient (p = 0.003). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9211364" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#19" class="mim-tip-reference" title="Webb, B. D., Brandt, T., Liu, L., Jalas, C., Liao, J., Fedick, A., Linderman, M. D., Diaz, G. A., Kornreich, R., Trachtman, H., Mehta, L., Edelmann, L. <strong>A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population.</strong> Clin. Genet. 86: 155-160, 2014.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/23927549/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">23927549</a>] [<a href="https://doi.org/10.1111/cge.12247" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="23927549">Webb et al. (2014)</a> reported a nonconsanguineous Ashkenazi Jewish family in which 3 sisters had ATS3B. The oldest developed hematuria and proteinuria at age 2 years. Renal biopsy at age 3 years showed irregular thickening of the GBM with splitting and reduplication of the lamina densa with a lace-like appearance. The second sister had asymptomatic microhematuria and proteinuria at age 2 years. Microscopy revealed dysmorphic red blood cells and red blood cell casts and the first morning urine sample. The third sister had hematuria at 1 year of age. All 3 had sensorineural hearing loss and used hearing aids. Parents had normal renal function and denied hearing loss. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=23927549" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p>In a study of 41 families with stringent criteria for Alport syndrome, <a href="#3" class="mim-tip-reference" title="Feingold, J., Bois, E., Chompret, A., Broyer, M., Gubler, M.-C., Grunfeld, J.-P. <strong>Genetic heterogeneity of Alport syndrome.</strong> Kidney Int. 27: 672-677, 1985.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/4010153/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">4010153</a>] [<a href="https://doi.org/10.1038/ki.1985.63" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="4010153">Feingold et al. (1985)</a> found 4 families in which autosomal recessive inheritance seemed likely because of parental consanguinity and unaffected parents. The criteria were proven for renal disease with hematuria in at least 2 relatives, neural hearing loss in at least 1 affected person, and evolution to renal failure in at least 1 affected person. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=4010153" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>As reviewed by <a href="#6" class="mim-tip-reference" title="Gubler, M.-C., Knebelmann, B., Beziau, A., Broyer, M., Pirson, Y., Haddoum, F., Kleppel, M. M., Antignac, C. <strong>Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.</strong> Kidney Int. 47: 1142-1147, 1995.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7783412/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7783412</a>] [<a href="https://doi.org/10.1038/ki.1995.163" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7783412">Gubler et al. (1995)</a>, autosomal recessive transmission of Alport syndrome was suggested for a small percent of kindreds because of the finding of parental consanguinity, absence of severe symptoms in parents, and equal severity of the disease in males and females. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7783412" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>The transmission pattern of ATS3B in the families reported by <a href="#15" class="mim-tip-reference" title="Mochizuki, T., Lemmink, H. H., Mariyama, M., Antignac, C., Gubler, M.-C., Pirson, Y., Verellen-Dumoulin, C., Chan, B., Schroder, C. H., Smeets, H. J., Reeders, S. T. <strong>Identification of mutations in the alpha-3(IV) and alpha-4(IV) collagen genes in autosomal recessive Alport syndrome.</strong> Nature Genet. 8: 77-81, 1994.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7987396/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7987396</a>] [<a href="https://doi.org/10.1038/ng0994-77" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7987396">Mochizuki et al. (1994)</a> was consistent with autosomal recessive inheritance. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7987396" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p>In affected members of 2 unrelated families with autosomal recessive Alport syndrome, <a href="#15" class="mim-tip-reference" title="Mochizuki, T., Lemmink, H. H., Mariyama, M., Antignac, C., Gubler, M.-C., Pirson, Y., Verellen-Dumoulin, C., Chan, B., Schroder, C. H., Smeets, H. J., Reeders, S. T. <strong>Identification of mutations in the alpha-3(IV) and alpha-4(IV) collagen genes in autosomal recessive Alport syndrome.</strong> Nature Genet. 8: 77-81, 1994.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7987396/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7987396</a>] [<a href="https://doi.org/10.1038/ng0994-77" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7987396">Mochizuki et al. (1994)</a> identified homozygous mutations (<a href="/entry/120070#0001">120070.0001</a>, <a href="/entry/120070#0002">120070.0002</a>) in the COL4A3 gene. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7987396" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#11" class="mim-tip-reference" title="Lemmink, H. H., Mochizuki, T., van den Heuvel, L. P. W. J., Schroder, C. H., Barrientos, A., Monnens, L. A. H., van Oost, B. A., Brunner, H. G., Reeders, S. T., Smeets, H. J. M. <strong>Mutations in the type IV collagen alpha-3 (COL4A3) gene in autosomal recessive Alport syndrome.</strong> Hum. Molec. Genet. 3: 1269-1273, 1994.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7987301/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7987301</a>] [<a href="https://doi.org/10.1093/hmg/3.8.1269" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7987301">Lemmink et al. (1994)</a> identified compound heterozygous nonsense mutations in the COL4A3 gene (<a href="/entry/120070#0002">120070.0002</a> and <a href="/entry/120070#0003">120070.0003</a>) in a patient with autosomal recessive Alport syndrome. Another variant (L36P) was identified, although it was determined not to be pathogenic. Autosomal recessive inheritance due to pathogenic COL4A3 mutations accounted for at least 13% of 22 Alport syndrome cases in this sample. All cases with COL4A3 mutations had renal histology and high-frequency hearing loss typical of the X-linked form of Alport syndrome. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7987301" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>In a family from Reunion Island with ATS3B, <a href="#10" class="mim-tip-reference" title="Knebelmann, B., Forestier, L., Drouot, L., Quinones, S., Chuet, C., Benessy, F., Saus, J., Antignac, C. <strong>Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome.</strong> Hum. Molec. Genet. 4: 675-679, 1995.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7633417/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7633417</a>] [<a href="https://doi.org/10.1093/hmg/4.4.675" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7633417">Knebelmann et al. (1995)</a> identified homozygosity for a splice mutation (<a href="/entry/120070#0006">120070.0006</a>) in the COL4A3 gene in 2 affected sibs. <a href="#4" class="mim-tip-reference" title="Finielz, P., Cartault, F., Chuet, C., Genin, R. <strong>Alport syndrome in Reunion Island: phenotypic heterogeneity of the recessive-autosomal form. (Letter)</strong> Nephron 79: 237 only, 1998.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9647515/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9647515</a>] [<a href="https://doi.org/10.1159/000045039" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9647515">Finielz et al. (1998)</a> identified this mutation in a further 4 families from Reunion Island. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=9647515+7633417" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#6" class="mim-tip-reference" title="Gubler, M.-C., Knebelmann, B., Beziau, A., Broyer, M., Pirson, Y., Haddoum, F., Kleppel, M. M., Antignac, C. <strong>Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.</strong> Kidney Int. 47: 1142-1147, 1995.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7783412/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7783412</a>] [<a href="https://doi.org/10.1038/ki.1995.163" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7783412">Gubler et al. (1995)</a> stated that up to 15% of Alport syndrome cases represent the autosomal recessive form due to mutations in either the COL4A3 or the COL4A4 gene. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7783412" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>In a nonconsanguineous Ashkenazi Jewish family with ATS3B, <a href="#19" class="mim-tip-reference" title="Webb, B. D., Brandt, T., Liu, L., Jalas, C., Liao, J., Fedick, A., Linderman, M. D., Diaz, G. A., Kornreich, R., Trachtman, H., Mehta, L., Edelmann, L. <strong>A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population.</strong> Clin. Genet. 86: 155-160, 2014.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/23927549/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">23927549</a>] [<a href="https://doi.org/10.1111/cge.12247" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="23927549">Webb et al. (2014)</a> identified homozygosity for an in-frame deletion of 8 amino acids (<a href="/entry/120070#0011">120070.0011</a>) in the COL4A3 gene. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=23927549" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><strong><em>Evidence of Digenic Inheritance</em></strong></p><p>
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Using massively parallel sequencing, <a href="#13" class="mim-tip-reference" title="Mencarelli, M. A., Heidet, L., Storey, H., van Geel, M., Knebelmann, B., Fallerini, C., Miglietti, N., Antonucci, M. F., Cetta, F., Sayer, J. A., van den Wijngaard, A., Yau, S., Mari, F., Bruttini, M., Ariani, F., Dahan, K., Smeets, B., Antignac, C., Flinter, F., Renieri, A. <strong>Evidence of digenic inheritance in Alport syndrome.</strong> J. Med. Genet. 52: 163-174, 2015.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/25575550/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">25575550</a>] [<a href="https://doi.org/10.1136/jmedgenet-2014-102822" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="25575550">Mencarelli et al. (2015)</a> identified 11 patients with Alport syndrome who had pathogenic mutations in 2 of the 3 collagen IV genes. Seven patients had a combination of mutations in COL4A3 (<a href="/entry/120070">120070</a>) and COL4A4 (<a href="/entry/120131">120131</a>). In 5 of these patients (families 1 through 5), the 2 mutations were inherited independently (like in trans), and in the other 2 (families 6 and 7) the mutations were inherited on the same chromosome (like in cis). In families 1 through 5 individuals with 2 heterozygous mutations had more severe phenotypes than those with a single heterozygous mutation. Individuals carrying a heterozygous mutation only in COL4A3 had hematuria. Individuals carrying a heterozygous mutation only in COL4A4 had phenotypes ranging from hematuria to end-stage renal disease. In families 6 and 7, the phenotype in individuals carrying 2 mutations was more severe than expected for the classic autosomal dominant form, with 1 affected individual from each of these families progressing toward end-stage renal disease at 40 years of age. <a href="#13" class="mim-tip-reference" title="Mencarelli, M. A., Heidet, L., Storey, H., van Geel, M., Knebelmann, B., Fallerini, C., Miglietti, N., Antonucci, M. F., Cetta, F., Sayer, J. A., van den Wijngaard, A., Yau, S., Mari, F., Bruttini, M., Ariani, F., Dahan, K., Smeets, B., Antignac, C., Flinter, F., Renieri, A. <strong>Evidence of digenic inheritance in Alport syndrome.</strong> J. Med. Genet. 52: 163-174, 2015.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/25575550/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">25575550</a>] [<a href="https://doi.org/10.1136/jmedgenet-2014-102822" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="25575550">Mencarelli et al. (2015)</a> remarked that this is later than the mean age expected in the autosomal recessive form of Alport syndrome (31 years), but earlier than expected in the autosomal dominant form (56 years). <a href="#13" class="mim-tip-reference" title="Mencarelli, M. A., Heidet, L., Storey, H., van Geel, M., Knebelmann, B., Fallerini, C., Miglietti, N., Antonucci, M. F., Cetta, F., Sayer, J. A., van den Wijngaard, A., Yau, S., Mari, F., Bruttini, M., Ariani, F., Dahan, K., Smeets, B., Antignac, C., Flinter, F., Renieri, A. <strong>Evidence of digenic inheritance in Alport syndrome.</strong> J. Med. Genet. 52: 163-174, 2015.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/25575550/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">25575550</a>] [<a href="https://doi.org/10.1136/jmedgenet-2014-102822" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="25575550">Mencarelli et al. (2015)</a> concluded that these observations fit well with the stoichiometry of the molecules of the triple helix. In double heterozygotes, about 75% of triple-helix molecules are expected to be defective, which is greater than 50% in heterozygotes and less than 100% in homozygotes or hemizygotes. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=25575550" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<a href="#14" class="mim-tip-reference" title="Milliner, D. S., Pierides, A. M., Holley, K. E. <strong>Renal transplantation in Alport's syndrome: anti-glomerular basement membrane glomerulonephritis in the allograft.</strong> Mayo Clin. Proc. 57: 35-43, 1982.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7033680/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7033680</a>]" pmid="7033680">Milliner et al. (1982)</a> estimated that approximately 1 to 5% of Alport patients who receive transplants develop a specific anti-GBM nephritis, subsequently leading to loss of the renal graft. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7033680" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#9" class="mim-tip-reference" title="Kalluri, R., Weber, M., Netzer, K. -O., Sun, M. J., Neilson, E. G., Hudson, B. G. <strong>COL4A5 gene deletion and production of post-transplant anti-alpha-3(IV) collagen alloantibodies in Alport syndrome.</strong> Kidney Int. 45: 721-726, 1994.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8196274/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8196274</a>] [<a href="https://doi.org/10.1038/ki.1994.96" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="8196274">Kalluri et al. (1994)</a> found that posttransplant anti-GBM alloantibodies from an X-linked Alport patient with complete COL4A5 gene deletion were specifically targeted to the COL4A3 chain. In further studies, <a href="#8" class="mim-tip-reference" title="Kalluri, R., van den Heuvel, L. P., Smeets, H. J. M., Schroder, C. H., Lemmink, H. H., Boutaud, A., Neilson, E. G., Hudson, B. G. <strong>A COL4A3 gene mutation and post-transplant anti-alpha-3(IV) collagen alloantibodies in Alport syndrome.</strong> Kidney Int. 47: 1199-1204, 1995.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7783419/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7783419</a>] [<a href="https://doi.org/10.1038/ki.1995.170" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7783419">Kalluri et al. (1995)</a> demonstrated posttransplant anti-COL4A3 alloantibodies in a patient with autosomal recessive Alport syndrome caused by deletion of the last 198 amino acids of the COL4A3. The absence of the COL4A3 chain in the GBM of patients with both these forms of Alport syndrome, due either to a failure of synthesis or a failure of assembly, presumably leads to a loss of immunologic tolerance for the COL4A3 NC1 domain in transplanted allografts. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=8196274+7783419" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>In a review of mutations that had been identified in the type IV collagen genes in patients with Alport syndrome, <a href="#12" class="mim-tip-reference" title="Lemmink, H. H., Schroder, C. H., Monnens, L. A. H., Smeets, H. J. M. <strong>The clinical spectrum of type IV collagen mutations.</strong> Hum. Mutat. 9: 477-499, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9195222/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9195222</a>] [<a href="https://doi.org/10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-#" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9195222">Lemmink et al. (1997)</a> found data on 46 patients with transplants, among whom there were 41 with a COL4A5 mutation, 4 with a COL4A3 mutation, and 1 with a COL4A4 mutation. All patients except 1 had juvenile Alport syndrome. In 9 patients with transplants (20% of the total number of transplants), a specific anti-GBM nephritis was detected. Of these 9, 8 carried large deletions or premature stop codons, which were predicted to result in COL4A3 or COL4A5 proteins truncated within the noncollagenous (NC) domain. The exception was a splice mutation in COL4A5 resulting in an mRNA without exon 38. Four patients identified with COL4A3 mutations had had transplants and 3 of them developed an anti-GBM nephritis. These data suggested that Alport syndrome patients with a type IV collagen mutation resulting in absence of the NC domain have an increased risk of developing anti-GBM nephritis after renal transplantation. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9195222" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#7" class="mim-tip-reference" title="Kalluri, R., Danoff, T. M., Okada, H., Neilson, E. G. <strong>Susceptibility to anti-glomerular basement membrane disease and Goodpasture syndrome is linked to MHC class II genes and the emergence of T cell-mediated immunity in mice.</strong> J. Clin. Invest. 100: 2263-2275, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9410904/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9410904</a>] [<a href="https://doi.org/10.1172/JCI119764" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9410904">Kalluri et al. (1997)</a> developed a new mouse model of human anti-GBM disease to characterize better the genetic determinants of cell-mediated injury. The findings in studies of the model suggested that anti-GBM antibodies in mice facilitate disease only in MHC haplotypes capable of generating nephritogenic lymphocytes with special T-cell repertoires. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9410904" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p><a href="#6" class="mim-tip-reference" title="Gubler, M.-C., Knebelmann, B., Beziau, A., Broyer, M., Pirson, Y., Haddoum, F., Kleppel, M. M., Antignac, C. <strong>Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.</strong> Kidney Int. 47: 1142-1147, 1995.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7783412/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7783412</a>] [<a href="https://doi.org/10.1038/ki.1995.163" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="7783412">Gubler et al. (1995)</a> used an immunofluorescence technique to analyze the distribution of different type IV collagen chains in renal and skin basement membranes of 12 Alport syndrome patients belonging to 11 unrelated kindreds in which autosomal recessive inheritance had been demonstrated (3 kindreds) or suggested by clinical and genealogic data (8 kindreds). The renal and skin distribution was normal in 1 patient with a COL4A4 mutation. A particular pattern of distribution was observed in the other patients: co-absence of alpha-3(IV), alpha-4(IV), and alpha-5(IV) chains in the glomerular basement membrane, and the presence of the alpha-5(IV) chain in a series of extraglomerular basement membranes, including capsular, collecting ducts, and epidermal basement membranes, a combination never observed in X-linked Alport syndrome. This immunohistochemical pattern correlated with the specific distribution of the 3 types of collagen IV chains within extraglomerular basement membranes. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7783412" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p><a href="#19" class="mim-tip-reference" title="Webb, B. D., Brandt, T., Liu, L., Jalas, C., Liao, J., Fedick, A., Linderman, M. D., Diaz, G. A., Kornreich, R., Trachtman, H., Mehta, L., Edelmann, L. <strong>A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population.</strong> Clin. Genet. 86: 155-160, 2014.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/23927549/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">23927549</a>] [<a href="https://doi.org/10.1111/cge.12247" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="23927549">Webb et al. (2014)</a> identified a homozygous 24-bp deletion in the COL4A3 gene (c.40_63del; <a href="/entry/120070#0011">120070.0011</a>) in 3 sisters, born of unrelated parents of Ashkenazi Jewish descent, with autosomal recessive Alport syndrome. Population analysis yielded a carrier frequency of 0.55% (1 in 183) among Ashkenazi Jewish individuals, and haplotype analysis indicated a founder effect. Functional studies of the variant were not performed, but the parents were unaffected, suggesting that heterozygosity for this mutation does not predispose to disease. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=23927549" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<a href="#Gubler1981" class="mim-tip-reference" title="Gubler, M., Levy, M., Broyer, M., Naizot, C., Gonzales, G., Perrin, D., Habib, R. <strong>Alport's syndrome: a report of 58 cases and a review of the literature.</strong> Am. J. Med. 70: 493-505, 1981.">Gubler et al. (1981)</a>; <a href="#van2000" class="mim-tip-reference" title="van der Loop, F. T. L., Heidet, L., Timmer, E. D. J., van den Bosch, B. J. C., Leinonen, A., Antignac, C., Jefferson, J. A., Maxwell, A. P., Monnens, L. A. H., Schroder, C. H., Smeets, H. J. M. <strong>Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation.</strong> Kidney Int. 58: 1870-1875, 2000.">van der Loop et al. (2000)</a>
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Boye, E., Mollet, G., Forestier, L., Cohen-Solal, L., Heidet, L., Cochat, P., Grunfeld, J.-P., Palcoux, J.-B., Gubler, M.-C., Antignac, C.
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<strong>Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.</strong>
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Am. J. Hum. Genet. 63: 1329-1340, 1998.
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Colville, D., Savige, J., Morfis, M., Ellis, J., Kerr, P., Agar, J., Fasset, R.
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<strong>Ocular manifestations of autosomal recessive Alport syndrome.</strong>
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Ophthal. Genet. 18: 119-128, 1997.
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[<a href="https://doi.org/10.3109/13816819709057125" target="_blank">Full Text</a>]
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<a id="Feingold1985" class="mim-anchor"></a>
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Feingold, J., Bois, E., Chompret, A., Broyer, M., Gubler, M.-C., Grunfeld, J.-P.
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<strong>Genetic heterogeneity of Alport syndrome.</strong>
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Kidney Int. 27: 672-677, 1985.
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[<a href="https://doi.org/10.1038/ki.1985.63" target="_blank">Full Text</a>]
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Finielz, P., Cartault, F., Chuet, C., Genin, R.
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<strong>Alport syndrome in Reunion Island: phenotypic heterogeneity of the recessive-autosomal form. (Letter)</strong>
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Nephron 79: 237 only, 1998.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9647515/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9647515</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9647515" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1159/000045039" target="_blank">Full Text</a>]
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Gubler, M., Levy, M., Broyer, M., Naizot, C., Gonzales, G., Perrin, D., Habib, R.
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<strong>Alport's syndrome: a report of 58 cases and a review of the literature.</strong>
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Am. J. Med. 70: 493-505, 1981.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7211891/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7211891</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7211891" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1016/0002-9343(81)90571-4" target="_blank">Full Text</a>]
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Gubler, M.-C., Knebelmann, B., Beziau, A., Broyer, M., Pirson, Y., Haddoum, F., Kleppel, M. M., Antignac, C.
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<strong>Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.</strong>
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Kidney Int. 47: 1142-1147, 1995.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7783412/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7783412</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7783412" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1038/ki.1995.163" target="_blank">Full Text</a>]
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Kalluri, R., Danoff, T. M., Okada, H., Neilson, E. G.
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<strong>Susceptibility to anti-glomerular basement membrane disease and Goodpasture syndrome is linked to MHC class II genes and the emergence of T cell-mediated immunity in mice.</strong>
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J. Clin. Invest. 100: 2263-2275, 1997.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9410904/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9410904</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9410904" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1172/JCI119764" target="_blank">Full Text</a>]
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Kalluri, R., van den Heuvel, L. P., Smeets, H. J. M., Schroder, C. H., Lemmink, H. H., Boutaud, A., Neilson, E. G., Hudson, B. G.
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<strong>A COL4A3 gene mutation and post-transplant anti-alpha-3(IV) collagen alloantibodies in Alport syndrome.</strong>
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Kidney Int. 47: 1199-1204, 1995.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7783419/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7783419</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7783419" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1038/ki.1995.170" target="_blank">Full Text</a>]
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Kalluri, R., Weber, M., Netzer, K. -O., Sun, M. J., Neilson, E. G., Hudson, B. G.
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<strong>COL4A5 gene deletion and production of post-transplant anti-alpha-3(IV) collagen alloantibodies in Alport syndrome.</strong>
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Kidney Int. 45: 721-726, 1994.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8196274/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8196274</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8196274" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1038/ki.1994.96" target="_blank">Full Text</a>]
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Knebelmann, B., Forestier, L., Drouot, L., Quinones, S., Chuet, C., Benessy, F., Saus, J., Antignac, C.
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<strong>Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome.</strong>
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Hum. Molec. Genet. 4: 675-679, 1995.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7633417/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7633417</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7633417" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1093/hmg/4.4.675" target="_blank">Full Text</a>]
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Lemmink, H. H., Mochizuki, T., van den Heuvel, L. P. W. J., Schroder, C. H., Barrientos, A., Monnens, L. A. H., van Oost, B. A., Brunner, H. G., Reeders, S. T., Smeets, H. J. M.
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<strong>Mutations in the type IV collagen alpha-3 (COL4A3) gene in autosomal recessive Alport syndrome.</strong>
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Hum. Molec. Genet. 3: 1269-1273, 1994.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7987301/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7987301</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7987301" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1093/hmg/3.8.1269" target="_blank">Full Text</a>]
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Lemmink, H. H., Schroder, C. H., Monnens, L. A. H., Smeets, H. J. M.
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<strong>The clinical spectrum of type IV collagen mutations.</strong>
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Hum. Mutat. 9: 477-499, 1997.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9195222/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9195222</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9195222" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-#" target="_blank">Full Text</a>]
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</p>
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<a id="13" class="mim-anchor"></a>
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<a id="Mencarelli2015" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Mencarelli, M. A., Heidet, L., Storey, H., van Geel, M., Knebelmann, B., Fallerini, C., Miglietti, N., Antonucci, M. F., Cetta, F., Sayer, J. A., van den Wijngaard, A., Yau, S., Mari, F., Bruttini, M., Ariani, F., Dahan, K., Smeets, B., Antignac, C., Flinter, F., Renieri, A.
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|
<strong>Evidence of digenic inheritance in Alport syndrome.</strong>
|
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J. Med. Genet. 52: 163-174, 2015.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/25575550/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">25575550</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=25575550" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1136/jmedgenet-2014-102822" target="_blank">Full Text</a>]
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<a id="14" class="mim-anchor"></a>
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<a id="Milliner1982" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Milliner, D. S., Pierides, A. M., Holley, K. E.
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<strong>Renal transplantation in Alport's syndrome: anti-glomerular basement membrane glomerulonephritis in the allograft.</strong>
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|
Mayo Clin. Proc. 57: 35-43, 1982.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7033680/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7033680</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7033680" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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</p>
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<a id="15" class="mim-anchor"></a>
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<a id="Mochizuki1994" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Mochizuki, T., Lemmink, H. H., Mariyama, M., Antignac, C., Gubler, M.-C., Pirson, Y., Verellen-Dumoulin, C., Chan, B., Schroder, C. H., Smeets, H. J., Reeders, S. T.
|
|
<strong>Identification of mutations in the alpha-3(IV) and alpha-4(IV) collagen genes in autosomal recessive Alport syndrome.</strong>
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Nature Genet. 8: 77-81, 1994.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7987396/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7987396</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7987396" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1038/ng0994-77" target="_blank">Full Text</a>]
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</p>
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<li>
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<a id="16" class="mim-anchor"></a>
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<a id="Passwell1981" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Passwell, J. H., David, R., Boichis, H., Herzfeld, S.
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<strong>Hereditary nephritis with associated defects in proximal renal tubular function.</strong>
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J. Pediat. 98: 85-87, 1981.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7452412/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7452412</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7452412" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1016/s0022-3476(81)80545-8" target="_blank">Full Text</a>]
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</p>
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</div>
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<li>
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<a id="17" class="mim-anchor"></a>
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<a id="Rhys1997" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Rhys, C., Snyers, B., Pirson, Y.
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<strong>Recurrent corneal erosion associated with Alport's syndrome.</strong>
|
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Kidney Int. 52: 208-211, 1997.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9211364/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9211364</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9211364" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1038/ki.1997.321" target="_blank">Full Text</a>]
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</p>
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</div>
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<li>
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<a id="18" class="mim-anchor"></a>
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<a id="van der Loop2000" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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van der Loop, F. T. L., Heidet, L., Timmer, E. D. J., van den Bosch, B. J. C., Leinonen, A., Antignac, C., Jefferson, J. A., Maxwell, A. P., Monnens, L. A. H., Schroder, C. H., Smeets, H. J. M.
|
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<strong>Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation.</strong>
|
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Kidney Int. 58: 1870-1875, 2000.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/11044206/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">11044206</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=11044206" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1111/j.1523-1755.2000.00358.x" target="_blank">Full Text</a>]
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<li>
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<a id="19" class="mim-anchor"></a>
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<a id="Webb2014" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Webb, B. D., Brandt, T., Liu, L., Jalas, C., Liao, J., Fedick, A., Linderman, M. D., Diaz, G. A., Kornreich, R., Trachtman, H., Mehta, L., Edelmann, L.
|
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<strong>A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population.</strong>
|
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Clin. Genet. 86: 155-160, 2014.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/23927549/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">23927549</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=23927549" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1111/cge.12247" target="_blank">Full Text</a>]
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</p>
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</div>
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</ol>
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<br />
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</div>
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<div>
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<a id="contributors" class="mim-anchor"></a>
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<span class="mim-text-font">
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<a href="#mimCollapseContributors" role="button" data-toggle="collapse"> Contributors: </a>
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</div>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
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<span class="mim-text-font">
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Ada Hamosh - updated : 7/10/2015
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</span>
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</div>
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</div>
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<div class="row collapse" id="mimCollapseContributors">
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<div class="col-lg-offset-2 col-md-offset-4 col-sm-offset-4 col-xs-offset-2 col-lg-6 col-md-6 col-sm-6 col-xs-6">
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<span class="mim-text-font">
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Cassandra L. Kniffin - updated : 6/1/2015<br>Cassandra L. Kniffin - updated : 10/23/2014<br>Cassandra L. Kniffin - reorganized : 5/27/2010<br>Cassandra L. Kniffin - updated : 5/21/2010<br>Victor A. McKusick - updated : 6/15/1999
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</span>
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</div>
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</div>
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</div>
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<div>
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<a id="creationDate" class="mim-anchor"></a>
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<div class="row">
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<div class="col-lg-2 col-md-2 col-sm-4 col-xs-4">
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<span class="text-nowrap mim-text-font">
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Creation Date:
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</span>
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</div>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
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<span class="mim-text-font">
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Victor A. McKusick : 6/2/1986
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</span>
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</div>
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</div>
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</div>
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<div>
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<a id="editHistory" class="mim-anchor"></a>
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<div class="row">
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<div class="col-lg-2 col-md-2 col-sm-4 col-xs-4">
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<span class="text-nowrap mim-text-font">
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<a href="#mimCollapseEditHistory" role="button" data-toggle="collapse"> Edit History: </a>
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</span>
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</div>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
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<span class="mim-text-font">
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alopez : 10/06/2023
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</span>
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</div>
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<div class="row collapse" id="mimCollapseEditHistory">
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<div class="col-lg-offset-2 col-md-offset-2 col-sm-offset-4 col-xs-offset-4 col-lg-6 col-md-6 col-sm-6 col-xs-6">
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<span class="mim-text-font">
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alopez : 10/06/2023<br>alopez : 10/06/2023<br>carol : 01/31/2019<br>alopez : 07/13/2015<br>alopez : 7/10/2015<br>carol : 6/9/2015<br>mcolton : 6/2/2015<br>ckniffin : 6/1/2015<br>carol : 10/24/2014<br>ckniffin : 10/23/2014<br>carol : 5/27/2010<br>ckniffin : 5/21/2010<br>carol : 3/14/2000<br>mgross : 6/22/1999<br>mgross : 6/16/1999<br>mgross : 6/15/1999<br>alopez : 7/30/1997<br>mark : 7/9/1997<br>mimadm : 11/12/1995<br>mark : 6/13/1995<br>terry : 10/25/1994<br>supermim : 3/16/1992<br>carol : 3/27/1991<br>carol : 3/14/1991
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</span>
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</div>
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</div>
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</div>
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</div>
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</div>
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</div>
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<div class="container visible-print-block">
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<h3>
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<span class="mim-font">
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<strong>#</strong> 620536
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</h3>
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<div>
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<h3>
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<span class="mim-font">
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ALPORT SYNDROME 3B, AUTOSOMAL RECESSIVE; ATS3B
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</span>
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</h3>
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</div>
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<div>
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<br />
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<p>
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<span class="mim-text-font">
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<strong>ORPHA:</strong> 88919;
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</span>
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</p>
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<div>
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<br />
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<div>
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<h4>
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<span class="mim-font">
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<strong>Phenotype-Gene Relationships</strong>
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</span>
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</h4>
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<div>
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<table class="table table-bordered table-condensed small mim-table-padding">
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<thead>
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<tr class="active">
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<th>
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Location
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</th>
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<th>
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Phenotype
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</th>
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<th>
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Phenotype <br /> MIM number
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</th>
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<th>
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Inheritance
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</th>
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<th>
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Phenotype <br /> mapping key
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</th>
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<th>
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Gene/Locus
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</th>
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<th>
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Gene/Locus <br /> MIM number
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</th>
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</tr>
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</thead>
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<tbody>
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<tr>
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<td>
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<span class="mim-font">
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2q36.3
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</span>
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</td>
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<td>
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<span class="mim-font">
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Alport syndrome 3B, autosomal recessive
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</span>
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</td>
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<td>
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<span class="mim-font">
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620536
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</span>
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</td>
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<td>
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<span class="mim-font">
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Autosomal recessive
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</span>
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</td>
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<td>
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<span class="mim-font">
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|
3
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</span>
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</td>
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<td>
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<span class="mim-font">
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COL4A3
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</span>
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</td>
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<td>
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<span class="mim-font">
|
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120070
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</span>
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</td>
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</tr>
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</tbody>
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</table>
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</div>
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</div>
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<div>
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<br />
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</div>
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<div>
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<h4>
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<span class="mim-font">
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<strong>TEXT</strong>
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</span>
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</h4>
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<span class="mim-text-font">
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<p>A number sign (#) is used with this entry because of evidence that autosomal recessive Alport syndrome-3B (ATS3B) is caused by homozygous or compound heterozygous mutation in the COL4A3 (120070) gene on chromosome 2q36.</p><p>Another form of autosomal recessive Alport syndrome (ATS2; 120131) results from homozygous or compound heterozygous mutation in the COL4A4 gene (120131) on chromosome 2q36.</p>
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</span>
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<div>
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<br />
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</div>
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<div>
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<h4>
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<span class="mim-font">
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<strong>Description</strong>
|
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</span>
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</h4>
|
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</div>
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<span class="mim-text-font">
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<p>Autosomal recessive Alport syndrome-3B (ATS3B) is a progressive hematuric glomerulonephritis characterized by glomerular basement membrane abnormalities. Sensorineural hearing loss and ocular manifestations may be present (summary by Boye et al., 1998). </p><p>For a general phenotypic description of Alport syndrome, see the X-linked dominant form (ATS1; 301050).</p>
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</span>
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<div>
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<br />
|
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</div>
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<div>
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<h4>
|
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<span class="mim-font">
|
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<strong>Clinical Features</strong>
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</span>
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</h4>
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</div>
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<span class="mim-text-font">
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<p>Passwell et al. (1981) described a girl, born of first-cousin parents, who presented in the first year of life with failure to thrive and was found to have nephritis and deafness. She showed the characteristic electron microscopic feature of Alport syndrome, including thickening and splitting of the basement membranes of both the glomeruli and the tubules into thin layers, with accumulation of electron dense particles within this network. The parents were unaffected, but 2 maternal uncles had chronic nephritis and neurosensory deafness. An unusual feature was Fanconi syndrome in the proband. </p><p>Mochizuki et al. (1994) reported 2 unrelated families with autosomal recessive Alport syndrome and mutation in the COL4A3 gene. In family VB, a brother and sister were affected. The girl developed hematuria at age 4 years and also had sensorineural deafness. She received a renal allograft at age 10 and developed antiglomerular basement membrane (GBM) nephritis 6 months later. Her brother had hematuria, deafness, and deteriorating renal function. The unaffected parents had no known consanguinity but originated from the same small village in the Netherlands. In consanguineous family DU, an 11-year-old Belgian girl developed proteinuria and microhematuria at age 7 years and end-stage renal disease at age 11 years. At age 11, she had renal transplant from her mother, and no rejection or anti-GBM nephritis had developed by age 16. At age 13, an audiogram showed bilateral sensorineural hearing loss. Both parents were unaffected and had normal renal function and urinalysis. </p><p>Knebelmann et al. (1995) studied a family (HO) from Reunion Island with autosomal recessive Alport syndrome and mutation in the COL4A3 gene. A brother and sister reached end-stage renal failure at 14 and 15 years of age, respectively. Both had sensorineural hearing loss requiring hearing aids; no ocular symptoms were found. The father and 2 brothers were asymptomatic, but the mother had intermittent microscopic hematuria. Finielz et al. (1998) identified the same mutation in 4 other families from Reunion Island. In 1 family, 3 individuals, all male, were involved. Two were placed on hemodialysis for end-stage renal disease at ages 28 and 26 years; the third, aged 13 years, had normal serum creatinine concentration values. The 3 other families, who were from a different town, had discovery of Alport syndrome at earlier ages ranging from 3 to 13 years on the basis of macroscopic hematuria and/or proteinuria, and in only 1 case was deafness evident. Males and females seemed to be equally involved (3 boys, 3 girls). End-stage renal failure occurred earlier (ages 14, 14, 18, and 15), unrelated to sex. Auditory impairment was a constant feature when evaluated; ocular impairment involved 1 patient only. </p><p>Colville et al. (1997) examined the eyes of a family with autosomal recessive Alport syndrome. Four of the 8 offspring of a consanguineous marriage had renal failure and deafness by the age of 20 years. Studies of linkage to the COL4A5 (303630)/COL4A6 (303631) locus yielded strongly negative lod scores (excluding the X-linked form), whereas linkage to an intragenic marker for the COL4A3/COL4A4 locus showed positive lod scores consistent with the autosomal recessive form. All 4 affected members had anterior lenticonus, and the 3 who were examined had a dot-and-fleck retinopathy. Colville et al. (1997) concluded that the ocular manifestations of autosomal recessive Alport syndrome are identical to those of the X-linked form. </p><p>To assess the prevalence of recurrent corneal erosion (RCE) in Alport syndrome, Rhys et al. (1997) surveyed 41 patients with Alport syndrome and renal failure and 67 control patients transplanted for another form of nephropathy. A history of RCE, first manifested between the ages of 12 and 21 years, was obtained in 7 Alport syndrome patients, 1 with probable autosomal recessive inheritance, but in only 1 control patient (p = 0.003). </p><p>Webb et al. (2014) reported a nonconsanguineous Ashkenazi Jewish family in which 3 sisters had ATS3B. The oldest developed hematuria and proteinuria at age 2 years. Renal biopsy at age 3 years showed irregular thickening of the GBM with splitting and reduplication of the lamina densa with a lace-like appearance. The second sister had asymptomatic microhematuria and proteinuria at age 2 years. Microscopy revealed dysmorphic red blood cells and red blood cell casts and the first morning urine sample. The third sister had hematuria at 1 year of age. All 3 had sensorineural hearing loss and used hearing aids. Parents had normal renal function and denied hearing loss. </p>
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<h4>
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<span class="mim-font">
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<strong>Inheritance</strong>
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</span>
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</h4>
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<span class="mim-text-font">
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<p>In a study of 41 families with stringent criteria for Alport syndrome, Feingold et al. (1985) found 4 families in which autosomal recessive inheritance seemed likely because of parental consanguinity and unaffected parents. The criteria were proven for renal disease with hematuria in at least 2 relatives, neural hearing loss in at least 1 affected person, and evolution to renal failure in at least 1 affected person. </p><p>As reviewed by Gubler et al. (1995), autosomal recessive transmission of Alport syndrome was suggested for a small percent of kindreds because of the finding of parental consanguinity, absence of severe symptoms in parents, and equal severity of the disease in males and females. </p><p>The transmission pattern of ATS3B in the families reported by Mochizuki et al. (1994) was consistent with autosomal recessive inheritance. </p>
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<h4>
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<span class="mim-font">
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<strong>Molecular Genetics</strong>
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</span>
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</h4>
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<span class="mim-text-font">
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<p>In affected members of 2 unrelated families with autosomal recessive Alport syndrome, Mochizuki et al. (1994) identified homozygous mutations (120070.0001, 120070.0002) in the COL4A3 gene. </p><p>Lemmink et al. (1994) identified compound heterozygous nonsense mutations in the COL4A3 gene (120070.0002 and 120070.0003) in a patient with autosomal recessive Alport syndrome. Another variant (L36P) was identified, although it was determined not to be pathogenic. Autosomal recessive inheritance due to pathogenic COL4A3 mutations accounted for at least 13% of 22 Alport syndrome cases in this sample. All cases with COL4A3 mutations had renal histology and high-frequency hearing loss typical of the X-linked form of Alport syndrome. </p><p>In a family from Reunion Island with ATS3B, Knebelmann et al. (1995) identified homozygosity for a splice mutation (120070.0006) in the COL4A3 gene in 2 affected sibs. Finielz et al. (1998) identified this mutation in a further 4 families from Reunion Island. </p><p>Gubler et al. (1995) stated that up to 15% of Alport syndrome cases represent the autosomal recessive form due to mutations in either the COL4A3 or the COL4A4 gene. </p><p>In a nonconsanguineous Ashkenazi Jewish family with ATS3B, Webb et al. (2014) identified homozygosity for an in-frame deletion of 8 amino acids (120070.0011) in the COL4A3 gene. </p><p><strong><em>Evidence of Digenic Inheritance</em></strong></p><p>
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Using massively parallel sequencing, Mencarelli et al. (2015) identified 11 patients with Alport syndrome who had pathogenic mutations in 2 of the 3 collagen IV genes. Seven patients had a combination of mutations in COL4A3 (120070) and COL4A4 (120131). In 5 of these patients (families 1 through 5), the 2 mutations were inherited independently (like in trans), and in the other 2 (families 6 and 7) the mutations were inherited on the same chromosome (like in cis). In families 1 through 5 individuals with 2 heterozygous mutations had more severe phenotypes than those with a single heterozygous mutation. Individuals carrying a heterozygous mutation only in COL4A3 had hematuria. Individuals carrying a heterozygous mutation only in COL4A4 had phenotypes ranging from hematuria to end-stage renal disease. In families 6 and 7, the phenotype in individuals carrying 2 mutations was more severe than expected for the classic autosomal dominant form, with 1 affected individual from each of these families progressing toward end-stage renal disease at 40 years of age. Mencarelli et al. (2015) remarked that this is later than the mean age expected in the autosomal recessive form of Alport syndrome (31 years), but earlier than expected in the autosomal dominant form (56 years). Mencarelli et al. (2015) concluded that these observations fit well with the stoichiometry of the molecules of the triple helix. In double heterozygotes, about 75% of triple-helix molecules are expected to be defective, which is greater than 50% in heterozygotes and less than 100% in homozygotes or hemizygotes. </p>
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</span>
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<h4>
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<span class="mim-font">
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<strong>Clinical Management</strong>
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</span>
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<span class="mim-text-font">
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<p><strong><em>Complications of Renal Transplantation</em></strong></p><p>
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Milliner et al. (1982) estimated that approximately 1 to 5% of Alport patients who receive transplants develop a specific anti-GBM nephritis, subsequently leading to loss of the renal graft. </p><p>Kalluri et al. (1994) found that posttransplant anti-GBM alloantibodies from an X-linked Alport patient with complete COL4A5 gene deletion were specifically targeted to the COL4A3 chain. In further studies, Kalluri et al. (1995) demonstrated posttransplant anti-COL4A3 alloantibodies in a patient with autosomal recessive Alport syndrome caused by deletion of the last 198 amino acids of the COL4A3. The absence of the COL4A3 chain in the GBM of patients with both these forms of Alport syndrome, due either to a failure of synthesis or a failure of assembly, presumably leads to a loss of immunologic tolerance for the COL4A3 NC1 domain in transplanted allografts. </p><p>In a review of mutations that had been identified in the type IV collagen genes in patients with Alport syndrome, Lemmink et al. (1997) found data on 46 patients with transplants, among whom there were 41 with a COL4A5 mutation, 4 with a COL4A3 mutation, and 1 with a COL4A4 mutation. All patients except 1 had juvenile Alport syndrome. In 9 patients with transplants (20% of the total number of transplants), a specific anti-GBM nephritis was detected. Of these 9, 8 carried large deletions or premature stop codons, which were predicted to result in COL4A3 or COL4A5 proteins truncated within the noncollagenous (NC) domain. The exception was a splice mutation in COL4A5 resulting in an mRNA without exon 38. Four patients identified with COL4A3 mutations had had transplants and 3 of them developed an anti-GBM nephritis. These data suggested that Alport syndrome patients with a type IV collagen mutation resulting in absence of the NC domain have an increased risk of developing anti-GBM nephritis after renal transplantation. </p><p>Kalluri et al. (1997) developed a new mouse model of human anti-GBM disease to characterize better the genetic determinants of cell-mediated injury. The findings in studies of the model suggested that anti-GBM antibodies in mice facilitate disease only in MHC haplotypes capable of generating nephritogenic lymphocytes with special T-cell repertoires. </p>
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</span>
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<div>
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<h4>
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<span class="mim-font">
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<strong>Pathogenesis</strong>
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</span>
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</h4>
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</div>
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<span class="mim-text-font">
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<p>Gubler et al. (1995) used an immunofluorescence technique to analyze the distribution of different type IV collagen chains in renal and skin basement membranes of 12 Alport syndrome patients belonging to 11 unrelated kindreds in which autosomal recessive inheritance had been demonstrated (3 kindreds) or suggested by clinical and genealogic data (8 kindreds). The renal and skin distribution was normal in 1 patient with a COL4A4 mutation. A particular pattern of distribution was observed in the other patients: co-absence of alpha-3(IV), alpha-4(IV), and alpha-5(IV) chains in the glomerular basement membrane, and the presence of the alpha-5(IV) chain in a series of extraglomerular basement membranes, including capsular, collecting ducts, and epidermal basement membranes, a combination never observed in X-linked Alport syndrome. This immunohistochemical pattern correlated with the specific distribution of the 3 types of collagen IV chains within extraglomerular basement membranes. </p>
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</span>
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<div>
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<h4>
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<span class="mim-font">
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<strong>Population Genetics</strong>
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</span>
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</h4>
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</div>
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<span class="mim-text-font">
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<p>Webb et al. (2014) identified a homozygous 24-bp deletion in the COL4A3 gene (c.40_63del; 120070.0011) in 3 sisters, born of unrelated parents of Ashkenazi Jewish descent, with autosomal recessive Alport syndrome. Population analysis yielded a carrier frequency of 0.55% (1 in 183) among Ashkenazi Jewish individuals, and haplotype analysis indicated a founder effect. Functional studies of the variant were not performed, but the parents were unaffected, suggesting that heterozygosity for this mutation does not predispose to disease. </p>
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</span>
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<div>
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<br />
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</div>
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<div>
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<h4>
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<span class="mim-font">
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<strong>See Also:</strong>
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</span>
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</h4>
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<span class="mim-text-font">
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Gubler et al. (1981); van der Loop et al. (2000)
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</span>
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<div>
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<br />
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</div>
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</div>
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<div>
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<h4>
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<span class="mim-font">
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<strong>REFERENCES</strong>
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</span>
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</h4>
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<div>
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<p />
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</div>
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<div>
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<ol>
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<li>
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<p class="mim-text-font">
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Boye, E., Mollet, G., Forestier, L., Cohen-Solal, L., Heidet, L., Cochat, P., Grunfeld, J.-P., Palcoux, J.-B., Gubler, M.-C., Antignac, C.
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<strong>Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.</strong>
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Am. J. Hum. Genet. 63: 1329-1340, 1998.
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[PubMed: 9792860]
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[Full Text: https://doi.org/10.1086/302106]
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Colville, D., Savige, J., Morfis, M., Ellis, J., Kerr, P., Agar, J., Fasset, R.
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<strong>Ocular manifestations of autosomal recessive Alport syndrome.</strong>
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Ophthal. Genet. 18: 119-128, 1997.
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Feingold, J., Bois, E., Chompret, A., Broyer, M., Gubler, M.-C., Grunfeld, J.-P.
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<strong>Genetic heterogeneity of Alport syndrome.</strong>
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Kidney Int. 27: 672-677, 1985.
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Finielz, P., Cartault, F., Chuet, C., Genin, R.
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<strong>Alport syndrome in Reunion Island: phenotypic heterogeneity of the recessive-autosomal form. (Letter)</strong>
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Nephron 79: 237 only, 1998.
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Gubler, M., Levy, M., Broyer, M., Naizot, C., Gonzales, G., Perrin, D., Habib, R.
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<strong>Alport's syndrome: a report of 58 cases and a review of the literature.</strong>
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Am. J. Med. 70: 493-505, 1981.
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Gubler, M.-C., Knebelmann, B., Beziau, A., Broyer, M., Pirson, Y., Haddoum, F., Kleppel, M. M., Antignac, C.
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<strong>Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.</strong>
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Kalluri, R., Danoff, T. M., Okada, H., Neilson, E. G.
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<strong>Susceptibility to anti-glomerular basement membrane disease and Goodpasture syndrome is linked to MHC class II genes and the emergence of T cell-mediated immunity in mice.</strong>
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J. Clin. Invest. 100: 2263-2275, 1997.
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Kalluri, R., van den Heuvel, L. P., Smeets, H. J. M., Schroder, C. H., Lemmink, H. H., Boutaud, A., Neilson, E. G., Hudson, B. G.
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<strong>A COL4A3 gene mutation and post-transplant anti-alpha-3(IV) collagen alloantibodies in Alport syndrome.</strong>
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Kidney Int. 47: 1199-1204, 1995.
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[PubMed: 7783419]
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[Full Text: https://doi.org/10.1038/ki.1995.170]
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Kalluri, R., Weber, M., Netzer, K. -O., Sun, M. J., Neilson, E. G., Hudson, B. G.
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<strong>COL4A5 gene deletion and production of post-transplant anti-alpha-3(IV) collagen alloantibodies in Alport syndrome.</strong>
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Kidney Int. 45: 721-726, 1994.
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[PubMed: 8196274]
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[Full Text: https://doi.org/10.1038/ki.1994.96]
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Knebelmann, B., Forestier, L., Drouot, L., Quinones, S., Chuet, C., Benessy, F., Saus, J., Antignac, C.
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<strong>Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome.</strong>
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Hum. Molec. Genet. 4: 675-679, 1995.
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[PubMed: 7633417]
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[Full Text: https://doi.org/10.1093/hmg/4.4.675]
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Lemmink, H. H., Mochizuki, T., van den Heuvel, L. P. W. J., Schroder, C. H., Barrientos, A., Monnens, L. A. H., van Oost, B. A., Brunner, H. G., Reeders, S. T., Smeets, H. J. M.
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<strong>Mutations in the type IV collagen alpha-3 (COL4A3) gene in autosomal recessive Alport syndrome.</strong>
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Hum. Molec. Genet. 3: 1269-1273, 1994.
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[PubMed: 7987301]
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[Full Text: https://doi.org/10.1093/hmg/3.8.1269]
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Lemmink, H. H., Schroder, C. H., Monnens, L. A. H., Smeets, H. J. M.
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<strong>The clinical spectrum of type IV collagen mutations.</strong>
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Hum. Mutat. 9: 477-499, 1997.
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[Full Text: https://doi.org/10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-#]
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Mencarelli, M. A., Heidet, L., Storey, H., van Geel, M., Knebelmann, B., Fallerini, C., Miglietti, N., Antonucci, M. F., Cetta, F., Sayer, J. A., van den Wijngaard, A., Yau, S., Mari, F., Bruttini, M., Ariani, F., Dahan, K., Smeets, B., Antignac, C., Flinter, F., Renieri, A.
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<strong>Evidence of digenic inheritance in Alport syndrome.</strong>
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J. Med. Genet. 52: 163-174, 2015.
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[PubMed: 25575550]
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[Full Text: https://doi.org/10.1136/jmedgenet-2014-102822]
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<p class="mim-text-font">
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Milliner, D. S., Pierides, A. M., Holley, K. E.
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<strong>Renal transplantation in Alport's syndrome: anti-glomerular basement membrane glomerulonephritis in the allograft.</strong>
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Mayo Clin. Proc. 57: 35-43, 1982.
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[PubMed: 7033680]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Mochizuki, T., Lemmink, H. H., Mariyama, M., Antignac, C., Gubler, M.-C., Pirson, Y., Verellen-Dumoulin, C., Chan, B., Schroder, C. H., Smeets, H. J., Reeders, S. T.
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<strong>Identification of mutations in the alpha-3(IV) and alpha-4(IV) collagen genes in autosomal recessive Alport syndrome.</strong>
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Nature Genet. 8: 77-81, 1994.
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[PubMed: 7987396]
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[Full Text: https://doi.org/10.1038/ng0994-77]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Passwell, J. H., David, R., Boichis, H., Herzfeld, S.
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<strong>Hereditary nephritis with associated defects in proximal renal tubular function.</strong>
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J. Pediat. 98: 85-87, 1981.
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[PubMed: 7452412]
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[Full Text: https://doi.org/10.1016/s0022-3476(81)80545-8]
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Rhys, C., Snyers, B., Pirson, Y.
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<strong>Recurrent corneal erosion associated with Alport's syndrome.</strong>
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Kidney Int. 52: 208-211, 1997.
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[PubMed: 9211364]
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[Full Text: https://doi.org/10.1038/ki.1997.321]
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van der Loop, F. T. L., Heidet, L., Timmer, E. D. J., van den Bosch, B. J. C., Leinonen, A., Antignac, C., Jefferson, J. A., Maxwell, A. P., Monnens, L. A. H., Schroder, C. H., Smeets, H. J. M.
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<strong>Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation.</strong>
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Kidney Int. 58: 1870-1875, 2000.
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[PubMed: 11044206]
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[Full Text: https://doi.org/10.1111/j.1523-1755.2000.00358.x]
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Webb, B. D., Brandt, T., Liu, L., Jalas, C., Liao, J., Fedick, A., Linderman, M. D., Diaz, G. A., Kornreich, R., Trachtman, H., Mehta, L., Edelmann, L.
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<strong>A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population.</strong>
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Clin. Genet. 86: 155-160, 2014.
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[PubMed: 23927549]
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[Full Text: https://doi.org/10.1111/cge.12247]
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Ada Hamosh - updated : 7/10/2015<br>Cassandra L. Kniffin - updated : 6/1/2015<br>Cassandra L. Kniffin - updated : 10/23/2014<br>Cassandra L. Kniffin - reorganized : 5/27/2010<br>Cassandra L. Kniffin - updated : 5/21/2010<br>Victor A. McKusick - updated : 6/15/1999
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Victor A. McKusick : 6/2/1986
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