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Entry
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- #602588 - BRANCHIOOTIC SYNDROME 1; BOS1
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- OMIM
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<p>
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<span class="h4">#602588</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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<a href="/clinicalSynopsis/602588"><strong>Clinical Synopsis</strong></a>
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<a href="/phenotypicSeries/PS602588"> <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="#cytogenetics">Cytogenetics</a>
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<a href="#mapping">Mapping</a>
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<a href="#molecularGenetics">Molecular 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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<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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<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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</a>
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</h4>
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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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</a>
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<div><a href="https://clinicaltrials.gov/search?cond=BRANCHIOOTIC SYNDROME" 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=10697&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/NBK1380/" 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.diseaseinfosearch.org/x/955" class="mim-tip-hint" title="Network of disease-specific advocacy organizations, universities, private companies, government agencies, and public policy organizations." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Genetic Alliance', 'domain': 'diseaseinfosearch.org'})">Genetic Alliance</a></div>
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<div><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=602588[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=52429" 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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<div><a href="https://www.possumcore.com/nuxeo/nxdoc/default/afdc8891-d908-47d0-bc19-330164e888aa/view_documents?source=omim" class="mim-tip-hint" title="A dysmorphology database of multiple malformations; metabolic, teratogenic, chromosomal, and skeletal syndromes; and their images." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'POSSUM', 'domain': 'possum.net.au'})">POSSUM</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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</div>
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<div class="col-lg-8 col-lg-pull-2 col-md-8 col-md-pull-2 col-sm-8 col-sm-pull-2 col-xs-12">
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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>SNOMEDCT:</strong> 764810000<br />
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<strong>ORPHA:</strong> 52429<br />
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<strong>DO:</strong> 0060232<br />
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">ICD+</a>
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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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602588
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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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BRANCHIOOTIC SYNDROME 1; BOS1
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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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<a id="alternativeTitles" class="mim-anchor"></a>
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<div>
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<p>
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<span class="mim-font">
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<em>Alternative titles; symbols</em>
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</span>
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</p>
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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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BO SYNDROME 1<br />
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BRANCHIOOTIC DYSPLASIA
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</span>
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</h4>
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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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<a id="includedTitles" class="mim-anchor"></a>
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<div>
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<p>
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<span class="mim-font">
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Other entities represented in this entry:
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</span>
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</p>
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</div>
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<div>
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<span class="h3 mim-font">
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ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED
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</span>
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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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<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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</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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<a href="/geneMap/8/335?start=-3&limit=10&highlight=335">
|
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8q13.3
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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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Anterior segment anomalies with or without cataract
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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/602588"> 602588 </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 dominant">AD</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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EYA1
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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/601653"> 601653 </a>
|
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</span>
|
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</td>
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</tr>
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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/8/335?start=-3&limit=10&highlight=335">
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8q13.3
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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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Branchiootic syndrome 1
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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/602588"> 602588 </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 dominant">AD</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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EYA1
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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/601653"> 601653 </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>
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<div>
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<div class="btn-group ">
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<a href="/clinicalSynopsis/602588" 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/PS602588" 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>
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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/602588" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Linear'})"> Linear </a></li>
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<li><a href="/graph/radial/602588" 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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<div>
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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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- Autosomal dominant <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/263681008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">263681008</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/771269000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">771269000</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0443147&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0443147</a>, <a href="https://bioportal.bioontology.org/search?q=C1867440&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1867440</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000006</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000006</a>]</span><br />
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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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<span class="h5 mim-font">
|
|
<strong> HEAD & NECK </strong>
|
|
</span>
|
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</div>
|
|
<div style="margin-left: 2em;">
|
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<div>
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<div>
|
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<span class="h5 mim-font">
|
|
<em> Face </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
- Retrognathia <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/109515000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">109515000</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0035353&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0035353</a>, <a href="https://bioportal.bioontology.org/search?q=C3494422&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C3494422</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000278" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000278</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000278" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000278</a>]</span> <a href="https://elementsofmorphology.nih.gov/index.cgi?tid=ede3aa3495baae8accf26d8f779302ba" target="_blank" class="small mim-tip-eom" title="<img src="https://elementsofmorphology.nih.gov/images/terms/Retrognathia-small.jpg"> <br/>Further Information: <a href="https://elementsofmorphology.nih.gov/index.cgi?tid=ede3aa3495baae8accf26d8f779302ba" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'EOM\', \'domain\': \'elementsofmorphology.nih.gov\'})">Elements of Morphology</a>"><span class="glyphicon glyphicon-user" aria-hidden="true"></span></a><br />
|
|
|
|
</span>
|
|
</div>
|
|
</div>
|
|
|
|
|
|
<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<em> Ears </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
- 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 /> -
|
|
Conductive hearing loss <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/44057004" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">44057004</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/H90.2" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">H90.2</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/389.00" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389.00</a>, <a href="https://purl.bioontology.org/ontology/ICD9CM/389.0" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389.0</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0018777&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0018777</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000405" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000405</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000405" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000405</a>]</span><br /> -
|
|
Mixed hearing loss <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/77507001" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">77507001</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/H90.8" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">H90.8</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/389.20" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389.20</a>, <a href="https://purl.bioontology.org/ontology/ICD9CM/389.2" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389.2</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0155552&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0155552</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000410" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000410</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000410" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000410</a>]</span><br /> -
|
|
Preauricular pits <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/1955003" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">1955003</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0266610&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0266610</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0004467" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0004467</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0004467" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0004467</a>]</span><br /> -
|
|
Microtia <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/35045004" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">35045004</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q17.2" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q17.2</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/744.23" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">744.23</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0152423&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0152423</a>, <a href="https://bioportal.bioontology.org/search?q=C1657142&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1657142</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008551" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008551</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008551" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008551</a>]</span><br /> -
|
|
Malformed pinnae <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1846460&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1846460</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000356" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000356</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000356" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000356</a>]</span><br /> -
|
|
Hypoplastic pinnae <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/35045004" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">35045004</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q17.2" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q17.2</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/744.23" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">744.23</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0152423&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0152423</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008551" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008551</a>]</span><br /> -
|
|
Cup-shaped ears <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1845447&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1845447</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000378" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000378</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000378" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000378</a>]</span><br /> -
|
|
Low-set ears <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/95515009" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">95515009</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q17.4" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q17.4</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0239234&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0239234</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000369" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000369</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000369" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000369</a>]</span> <a href="https://elementsofmorphology.nih.gov/index.cgi?tid=9f0956aaa4fd45c34f94336afbbdc931" target="_blank" class="small mim-tip-eom" title="<img src="https://elementsofmorphology.nih.gov/images/terms/Ear,Low-Set-small.jpg"> <br/>Further Information: <a href="https://elementsofmorphology.nih.gov/index.cgi?tid=9f0956aaa4fd45c34f94336afbbdc931" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'EOM\', \'domain\': \'elementsofmorphology.nih.gov\'})">Elements of Morphology</a>"><span class="glyphicon glyphicon-user" aria-hidden="true"></span></a><br /> -
|
|
Narrowed external ear canal <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C2676971&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C2676971</a>]</span><br /> -
|
|
Unconnected or fused stapes and incus <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C2676972&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C2676972</a>]</span><br /> -
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Stapes fixation <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1861326&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1861326</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000381" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000381</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000381" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000381</a>]</span><br /> -
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Bulbous internal auditory canal <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C2676973&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C2676973</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0004458" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0004458</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0004458" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0004458</a>]</span><br /> -
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Cochlear malformation <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1862050&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1862050</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008554" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008554</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008554" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008554</a>]</span><br /> -
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Hypoplastic cochlea <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C2676974&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C2676974</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008586" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008586</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008586" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008586</a>]</span><br />
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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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<span class="h5 mim-font">
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<em> Neck </em>
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</span>
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</div>
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<div style="margin-left: 2em;">
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<span class="mim-font">
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- Branchial cleft fistulas or cysts, usually bilateral <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1862053&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1862053</a>]</span><br />
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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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<span class="h5 mim-font">
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<strong> MISCELLANEOUS </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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- Variable expressivity <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1861403&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1861403</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003828" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003828</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003828" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003828</a>]</span><br /> -
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Incomplete penetrance <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1836598&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1836598</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003829" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003829</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003829" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003829</a>]</span><br /> -
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Genetic heterogeneity, see BOS2 (<a href="/entry/120502">120502</a>) and BOS3 (<a href="/entry/608389">608389</a>)<br /> -
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Onset of hearing loss ranges from childhood to young adulthood<br /> -
|
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Allelic disorder to branchiootorenal syndrome (BOR, <a href="/entry/113650">113650</a>) and otofaciocervical syndrome (<a href="/entry/166780">166780</a>)<br />
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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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<span class="h5 mim-font">
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<strong> MOLECULAR BASIS </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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- Caused by mutation in the EYA transcriptional coactivator and phosphatase 1 gene (EYA1, <a href="/entry/601653#0003">601653.0003</a>)<br />
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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 class="text-right">
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<a href="#mimClinicalSynopsisFold" data-toggle="collapse">▲ Close</a>
|
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</div>
|
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</div>
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</div>
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<div id="mimPhenotypicSeriesFold" class="well well-sm collapse mimSingletonToggleFold">
|
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<div class="small">
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<div class="row">
|
|
<div class="col-lg-12 col-md-12 col-sm-12 col-xs-12">
|
|
<h5>
|
|
Branchiootic syndrome
|
|
- <a href="/phenotypicSeries/PS602588">PS602588</a>
|
|
- 4 Entries
|
|
</h5>
|
|
</div>
|
|
</div>
|
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|
|
<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/1/1503?start=-3&limit=10&highlight=1503"> 1q31 </a>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/120502"> Branchiootic syndrome 2 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/120502"> 120502 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/120502"> BOS2 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/120502"> 120502 </a>
|
|
</span>
|
|
</td>
|
|
</tr>
|
|
|
|
<tr>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<a href="/geneMap/8/335?start=-3&limit=10&highlight=335"> 8q13.3 </a>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/602588"> Anterior segment anomalies with or without cataract </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</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/602588"> 602588 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/601653"> EYA1 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/601653"> 601653 </a>
|
|
</span>
|
|
</td>
|
|
</tr>
|
|
|
|
<tr>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<a href="/geneMap/8/335?start=-3&limit=10&highlight=335"> 8q13.3 </a>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/602588"> Branchiootic syndrome 1 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</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/602588"> 602588 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/601653"> EYA1 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/601653"> 601653 </a>
|
|
</span>
|
|
</td>
|
|
</tr>
|
|
|
|
<tr>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<a href="/geneMap/14/287?start=-3&limit=10&highlight=287"> 14q23.1 </a>
|
|
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/608389"> Branchiootic syndrome 3 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
|
|
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</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/608389"> 608389 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/601205"> SIX1 </a>
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
<a href="/entry/601205"> 601205 </a>
|
|
</span>
|
|
</td>
|
|
</tr>
|
|
|
|
</tbody>
|
|
</table>
|
|
</div>
|
|
|
|
|
|
|
|
|
|
|
|
|
|
<div class="text-right small">
|
|
<a href="#mimPhenotypicSeriesFold" data-toggle="collapse">▲ Close</a>
|
|
</div>
|
|
</div>
|
|
</div>
|
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|
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</div>
|
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|
|
<div>
|
|
<br />
|
|
</div>
|
|
|
|
|
|
|
|
<div>
|
|
<a id="text" class="mim-anchor"></a>
|
|
|
|
|
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|
|
<h4 href="#mimTextFold" id="mimTextToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
|
|
<span id="mimTextToggleTriangle" class="small mimTextToggleTriangle">▼</span>
|
|
|
|
<span class="mim-font">
|
|
<span class="mim-tip-floating" qtip_title="<strong>Looking For More References?</strong>" qtip_text="Click the 'reference plus' icon <span class='glyphicon glyphicon-plus-sign'></span> at the end of each OMIM text paragraph to see more references related to the content of the preceding paragraph.">
|
|
<strong>TEXT</strong>
|
|
</span>
|
|
</span>
|
|
</h4>
|
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|
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<div id="mimTextFold" class="collapse in ">
|
|
<span class="mim-text-font">
|
|
<p>A number sign (#) is used with this entry because of evidence that branchiootic syndrome-1 (BOS1) is caused by heterozygous mutation in the EYA1 gene (<a href="/entry/601653">601653</a>) on chromosome 8q13.</p><p>Anterior segment anomalies with or without cataract is also caused by heterozygous mutation in the EYA1 gene.</p>
|
|
</span>
|
|
<div>
|
|
<br />
|
|
</div>
|
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</div>
|
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|
|
|
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<div>
|
|
<a id="description" class="mim-anchor"></a>
|
|
<h4 href="#mimDescriptionFold" id="mimDescriptionToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
|
|
<span id="mimDescriptionToggleTriangle" class="small mimTextToggleTriangle">▼</span>
|
|
<span class="mim-font">
|
|
<strong>Description</strong>
|
|
</span>
|
|
</h4>
|
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</div>
|
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|
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<div id="mimDescriptionFold" class="collapse in ">
|
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<span class="mim-text-font">
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<p>Individuals with the branchiootic syndrome (BOS) are affected by the same branchial and otic anomalies as those seen in individuals with the branchiootorenal syndrome (see BOR1, <a href="/entry/113650">113650</a>), but lack renal anomalies (<a href="#16" class="mim-tip-reference" title="Vincent, C., Kalatzis, V., Abdelhak, S., Chaib, H., Compain, S., Helia, J., Vaneecloo, F.-M., Petit, C. <strong>BOR and BO syndromes are allelic defects of EYA1.</strong> Europ. J. Hum. Genet. 5: 242-246, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9359046/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9359046</a>]" pmid="9359046">Vincent et al., 1997</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9359046" 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>Although <a href="#12" class="mim-tip-reference" title="Melnick, M., Hodes, M. E., Nance, W. E., Yune, H., Sweeney, A. <strong>Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.</strong> Clin. Genet. 13: 425-442, 1978.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/657583/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">657583</a>] [<a href="https://doi.org/10.1111/j.1399-0004.1978.tb04142.x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="657583">Melnick et al. (1978)</a> maintained that the BO syndrome is distinct from the BOR syndrome because of the lack of renal anomalies and variable presence of deafness in the former, <a href="#3" class="mim-tip-reference" title="Cremers, C. W. R. J., Fikkers-Van Noord, M. <strong>The earpits-deafness syndrome: clinical and genetic aspects.</strong> Int. J. Pediat. Otorhinolaryng. 2: 309-322, 1980.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/6964893/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">6964893</a>] [<a href="https://doi.org/10.1016/0165-5876(80)90036-1" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="6964893">Cremers and Fikkers-van Noord (1980)</a> suggested that the 2 syndromes represent a single entity. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=657583+6964893" 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>See <a href="/entry/113600">113600</a> for a discussion of branchial cleft anomalies, which may be related.</p><p><strong><em>Genetic Heterogeneity of Branchiootic Syndrome</em></strong></p><p>
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See also BOS2 (<a href="/entry/120502">120502</a>), mapped to chromosome 1, and BOS3 (<a href="/entry/608389">608389</a>), caused by mutation in the SIX1 gene (<a href="/entry/601205">601205</a>) on chromosome 14q23.</p>
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<p><a href="#6" class="mim-tip-reference" title="Fourman, P., Fourman, J. <strong>Hereditary deafness in family with ear-pits (fistula auris congenita).</strong> Brit. Med. J. 2: 1354-1356, 1955.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/13269867/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">13269867</a>] [<a href="https://doi.org/10.1136/bmj.2.4952.1354" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="13269867">Fourman and Fourman (1955)</a> described a large multigenerational family in which 17 members had preauricular pits, 12 of whom also had mild to severe sensorineural hearing loss. Among family members without preauricular pits, 3 had hearing loss: one of these individuals had a branchial pit. Some reported onset of hearing loss in childhood, whereas others had onset beginning at about age 20 years. Audiograms showed both high and low tone loss, usually high tone more than low. There was no evidence of vestibular disorder. The authors suggested that ear pits, deafness, and branchial fistulae were independent effects of a single dominant gene with incomplete penetrance. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=13269867" 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="#17" class="mim-tip-reference" title="Wildervanck, L. S. <strong>Hereditary malformations of the ear in three generations.</strong> Acta Otolaryng. 54: 553-560, 1962.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/14006981/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">14006981</a>] [<a href="https://doi.org/10.3109/00016486209126973" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="14006981">Wildervanck (1962)</a> reported a family in which 14 members had either deformed auricles, marginal pits, or preauricular appendages. Two had a moderate conductive deafness: bilateral in 1 and unilateral in the other. The mode of inheritance was dominant with full penetration. <a href="#17" class="mim-tip-reference" title="Wildervanck, L. S. <strong>Hereditary malformations of the ear in three generations.</strong> Acta Otolaryng. 54: 553-560, 1962.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/14006981/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">14006981</a>] [<a href="https://doi.org/10.3109/00016486209126973" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="14006981">Wildervanck (1962)</a> suggested this was a different syndrome from that described by <a href="#6" class="mim-tip-reference" title="Fourman, P., Fourman, J. <strong>Hereditary deafness in family with ear-pits (fistula auris congenita).</strong> Brit. Med. J. 2: 1354-1356, 1955.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/13269867/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">13269867</a>] [<a href="https://doi.org/10.1136/bmj.2.4952.1354" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="13269867">Fourman and Fourman (1955)</a>. <a href="#11" class="mim-tip-reference" title="McLaurin, J. W., Kloepfer, H. W., Laguaite, J. K., Stallcup, T. A. <strong>Hereditary branchial anomalies and associated hearing impairment.</strong> Laryngoscope 76: 1277-1288, 1966."None>McLaurin et al. (1966)</a> reported a kindred with branchial anomalies and associated hearing impairment similar to the kindred described by <a href="#17" class="mim-tip-reference" title="Wildervanck, L. S. <strong>Hereditary malformations of the ear in three generations.</strong> Acta Otolaryng. 54: 553-560, 1962.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/14006981/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">14006981</a>] [<a href="https://doi.org/10.3109/00016486209126973" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="14006981">Wildervanck (1962)</a>. <a href="#2" class="mim-tip-reference" title="Brusis, T. <strong>Gleichzeitiges Vorkommen von degenerativer Innenohrschwerhoerigheit, Vestibularisstoerung, beiderseitigen Ohr-und lateralen Halsfisteln bei mehreren Mitgliedern einer Familie.</strong> Laryng. Rhinol. Otol. 53: 131-139, 1974."None>Brusis (1974)</a> reported a kindred similar to the one described by <a href="#6" class="mim-tip-reference" title="Fourman, P., Fourman, J. <strong>Hereditary deafness in family with ear-pits (fistula auris congenita).</strong> Brit. Med. J. 2: 1354-1356, 1955.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/13269867/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">13269867</a>] [<a href="https://doi.org/10.1136/bmj.2.4952.1354" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="13269867">Fourman and Fourman (1955)</a>. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=14006981+13269867" 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="#16" class="mim-tip-reference" title="Vincent, C., Kalatzis, V., Abdelhak, S., Chaib, H., Compain, S., Helia, J., Vaneecloo, F.-M., Petit, C. <strong>BOR and BO syndromes are allelic defects of EYA1.</strong> Europ. J. Hum. Genet. 5: 242-246, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9359046/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9359046</a>]" pmid="9359046">Vincent et al. (1997)</a> reported 2 families with the BO syndrome. Clinical features included branchial cervical fistulae, cup-shaped pinnae, preauricular pits, and sensorineural, conductive, or mixed hearing loss. There was no evidence of renal anomalies. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9359046" 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="#14" class="mim-tip-reference" title="Spruijt, L., Hoefsloot, L. H., van Schaijk, G. H. W. H., van Waardenburg, D., Kremer, B., Brackel, H. J. L., de Die-Smulders, C. E. M. <strong>Identification of a novel EYA1 mutation presenting in a newborn with laryngomalacia, glossoptosis, retrognathia, and pectus excavatum. (Letter)</strong> Am. J. Med. Genet. 140A: 1343-1345, 2006.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/16691597/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">16691597</a>] [<a href="https://doi.org/10.1002/ajmg.a.31285" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="16691597">Spruijt et al. (2006)</a> reported an infant with severe obstructive sleep apnea caused by laryngomalacia, pharyngomalacia, glossoptosis, and tracheobronchomalacia. He also had bilateral branchial fistulae and ear anomalies, including ear pits, simple helices, and slight cup-shaped and low-set left ear. The features suggested BO syndrome. Other findings included micro- and retrognathia, but kidneys and hearing were normal. Surgical intervention improved the upper airway obstruction, but mild delay and mental and motor development were observed at age 11 months. His mildly affected mother showed mild retrognathia, left-sided branchial neck fistula, left-sided preauricular pit, and right-sided branchial cyst in the neck. Kidney ultrasound and hearing were normal. Both mother and son were heterozygous for a truncating mutation in the EYA1 gene (<a href="/entry/601653#0015">601653.0015</a>). <a href="#14" class="mim-tip-reference" title="Spruijt, L., Hoefsloot, L. H., van Schaijk, G. H. W. H., van Waardenburg, D., Kremer, B., Brackel, H. J. L., de Die-Smulders, C. E. M. <strong>Identification of a novel EYA1 mutation presenting in a newborn with laryngomalacia, glossoptosis, retrognathia, and pectus excavatum. (Letter)</strong> Am. J. Med. Genet. 140A: 1343-1345, 2006.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/16691597/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">16691597</a>] [<a href="https://doi.org/10.1002/ajmg.a.31285" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="16691597">Spruijt et al. (2006)</a> emphasized the phenotypic variability of BO syndrome associated with EYA1 mutations. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=16691597" 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="#8" class="mim-tip-reference" title="Haan, E. A., Hull, Y. J., White, S., Cockington, R., Charlton, P., Callen, D. F. <strong>Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.</strong> Am. J. Med. Genet. 32: 490-494, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2773990/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2773990</a>] [<a href="https://doi.org/10.1002/ajmg.1320320412" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2773990">Haan et al. (1989)</a> reported a complex inherited rearrangement of chromosome 8q associated with both trichorhinophalangeal syndrome (TRPS1; <a href="/entry/190350">190350</a>) and the BO syndrome in an affected Australian family showing features of both disorders. Preauricular pits or branchial sinuses were present in all 8 members studied in detail; 7 of these had deafness, the exception being the youngest. Three breakpoints in 8q were identified, resulting in dir ins(8)(q24.11q13.3q21.13). One of them was consistent with the previously assigned location of the TRPS1 locus on 8q24. <a href="#8" class="mim-tip-reference" title="Haan, E. A., Hull, Y. J., White, S., Cockington, R., Charlton, P., Callen, D. F. <strong>Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.</strong> Am. J. Med. Genet. 32: 490-494, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2773990/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2773990</a>] [<a href="https://doi.org/10.1002/ajmg.1320320412" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2773990">Haan et al. (1989)</a> concluded that the BO syndrome is caused by mutation at either 8q13.3 or 8q21.13. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=2773990" 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="Gu, J. Z., Wagner, M. J., Haan, E. A., Wells, D. E. <strong>Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): implications for mapping and cloning of the BOR gene.</strong> Genomics 31: 201-206, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8824802/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8824802</a>] [<a href="https://doi.org/10.1006/geno.1996.0032" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="8824802">Gu et al. (1996)</a> made use of a cell line from one of the affected members of the family reported by <a href="#8" class="mim-tip-reference" title="Haan, E. A., Hull, Y. J., White, S., Cockington, R., Charlton, P., Callen, D. F. <strong>Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.</strong> Am. J. Med. Genet. 32: 490-494, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2773990/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2773990</a>] [<a href="https://doi.org/10.1002/ajmg.1320320412" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2773990">Haan et al. (1989)</a>. YACs spanning the BO interval from D8S543 to D8S541 were used as fluorescence in situ hybridization probes. In addition to the cytogenetically defined direct insertion of material from 8q13.3-q21.13 into 8q24.11, a previously unidentified deletion of just under 1 megabase was found in 8q13.3. These data narrowed the most likely location of the BO gene to a region between D8S543 and D8S279. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=2773990+8824802" 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="Kalatzis, V., Abdelhak, S., Compain, S., Vincent, C., Petit, C. <strong>Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndrome.</strong> Genomics 34: 422-425, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8786145/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8786145</a>] [<a href="https://doi.org/10.1006/geno.1996.0307" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="8786145">Kalatzis et al. (1996)</a> likewise used the cell line first described by <a href="#8" class="mim-tip-reference" title="Haan, E. A., Hull, Y. J., White, S., Cockington, R., Charlton, P., Callen, D. F. <strong>Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.</strong> Am. J. Med. Genet. 32: 490-494, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2773990/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2773990</a>] [<a href="https://doi.org/10.1002/ajmg.1320320412" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2773990">Haan et al. (1989)</a> and identified an associated deletion by fluorescence in situ hybridization analysis of the 8q translocation breakpoint. The generation of a YAC contig and the isolation of overlapping recombinant P1 and lambda phage clones from the region allowed further characterization of the deletion. Its size was estimated to be between 470 and 650 kb, and it was flanked by the polymorphic markers D8S1060 and D8S1807. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=2773990+8786145" 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="#16" class="mim-tip-reference" title="Vincent, C., Kalatzis, V., Abdelhak, S., Chaib, H., Compain, S., Helia, J., Vaneecloo, F.-M., Petit, C. <strong>BOR and BO syndromes are allelic defects of EYA1.</strong> Europ. J. Hum. Genet. 5: 242-246, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9359046/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9359046</a>]" pmid="9359046">Vincent et al. (1997)</a> analyzed 2 large independent families in which each of the 8 affected members presented exclusively with BO syndrome. In both families, linkage analysis mapped the causative gene to the same region on chromosome 8q13.3. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9359046" 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>Genetic Heterogeneity</em></strong></p><p>
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<a href="#15" class="mim-tip-reference" title="Stratakis, C. A., Lin, J. P., Rennert, O. M. <strong>Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).</strong> Am. J. Med. Genet. 79: 209-214, 1998.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9788564/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9788564</a>]" pmid="9788564">Stratakis et al. (1998)</a> excluded linkage to 8q13.3 in a large family with presumed autosomal dominant BO syndrome spanning 4 generations. Ear pits were present in all 15 patients, whereas hearing loss and other branchial arch anomalies were present in 40% and 20%, respectively. None of the affected members had renal abnormalities or lacrimal duct stenosis. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9788564" 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="#16" class="mim-tip-reference" title="Vincent, C., Kalatzis, V., Abdelhak, S., Chaib, H., Compain, S., Helia, J., Vaneecloo, F.-M., Petit, C. <strong>BOR and BO syndromes are allelic defects of EYA1.</strong> Europ. J. Hum. Genet. 5: 242-246, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9359046/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9359046</a>]" pmid="9359046">Vincent et al. (1997)</a> demonstrated a 2-bp insertion in the EYA1 gene (<a href="/entry/601653#0003">601653.0003</a>) in 1 of 2 families with BO syndrome. In the other family, they detected an 8-bp deletion (<a href="/entry/601653#0004">601653.0004</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9359046" 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="#14" class="mim-tip-reference" title="Spruijt, L., Hoefsloot, L. H., van Schaijk, G. H. W. H., van Waardenburg, D., Kremer, B., Brackel, H. J. L., de Die-Smulders, C. E. M. <strong>Identification of a novel EYA1 mutation presenting in a newborn with laryngomalacia, glossoptosis, retrognathia, and pectus excavatum. (Letter)</strong> Am. J. Med. Genet. 140A: 1343-1345, 2006.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/16691597/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">16691597</a>] [<a href="https://doi.org/10.1002/ajmg.a.31285" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="16691597">Spruijt et al. (2006)</a> identified a heterozygous mutation in the EYA1 gene (<a href="/entry/601653#0014">601653.0014</a>) in an infant with a variant form of BO syndrome. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=16691597" 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>Anterior Segment Anomalies with or without Cataract</em></strong></p><p>
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<a href="#1" class="mim-tip-reference" title="Azuma, N., Hirakiyama, A., Inoue, T., Asaka, A., Yamada, M. <strong>Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies.</strong> Hum. Molec. Genet. 9: 363-366, 2000.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10655545/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10655545</a>] [<a href="https://doi.org/10.1093/hmg/9.3.363" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10655545">Azuma et al. (2000)</a> examined genomic DNA isolated from patients with various types of developmental eye anomalies for EYA1 mutations by use of PCR-SSCP and sequencing. They identified 3 novel missense mutations in patients who had congenital cataracts and ocular anterior segment anomalies (see, e.g., <a href="/entry/601653#0008">601653.0008</a>-<a href="/entry/601653#0009">601653.0009</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10655545" 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="#Cremers1981" class="mim-tip-reference" title="Cremers, C. W. R. J., Thijssen, H. O. M., Fischer, A. J. E. M., Marres, E. H. M. A. <strong>Otological aspects of the earpit-deafness syndrome.</strong> ORL 43: 223-239, 1981.">Cremers et al. (1981)</a>; <a href="#Fitch1976" class="mim-tip-reference" title="Fitch, N., Lindsay, J. R., Srolovitz, H. <strong>The temporal bone in the preauricular pit, cervical fistula, hearing loss syndrome.</strong> Ann. Otol. Rhinol. Laryng. 85: 268-275, 1976.">Fitch et al. (1976)</a>; <a href="#Hoskins2007" class="mim-tip-reference" title="Hoskins, B. E., Cramer, C. H., II, Silvius, D., Zou, D., Raymond, R. M., Jr., Orten, D. J., Kimberling, W. J., Smith, R. J. H., Weil, D., Petit, C., Otto, E. A., Xu, P.-X., Hildebrandt, F. <strong>Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome.</strong> Am. J. Hum. Genet. 80: 800-804, 2007.">Hoskins et al. (2007)</a>; <a href="#Rowley1969" class="mim-tip-reference" title="Rowley, P. T. <strong>Familial hearing loss associated with branchial fistulas.</strong> Pediatrics 44: 978-985, 1969.">Rowley (1969)</a>
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Azuma, N., Hirakiyama, A., Inoue, T., Asaka, A., Yamada, M.
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<strong>Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies.</strong>
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Hum. Molec. Genet. 9: 363-366, 2000.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10655545/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10655545</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10655545" 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/9.3.363" target="_blank">Full Text</a>]
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Brusis, T.
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<strong>Gleichzeitiges Vorkommen von degenerativer Innenohrschwerhoerigheit, Vestibularisstoerung, beiderseitigen Ohr-und lateralen Halsfisteln bei mehreren Mitgliedern einer Familie.</strong>
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Laryng. Rhinol. Otol. 53: 131-139, 1974.
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Cremers, C. W. R. J., Fikkers-Van Noord, M.
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<strong>The earpits-deafness syndrome: clinical and genetic aspects.</strong>
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Int. J. Pediat. Otorhinolaryng. 2: 309-322, 1980.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/6964893/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">6964893</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=6964893" 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/10.1016/0165-5876(80)90036-1" target="_blank">Full Text</a>]
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<a id="Cremers1981" class="mim-anchor"></a>
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Cremers, C. W. R. J., Thijssen, H. O. M., Fischer, A. J. E. M., Marres, E. H. M. A.
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<strong>Otological aspects of the earpit-deafness syndrome.</strong>
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ORL 43: 223-239, 1981.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/6973119/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">6973119</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=6973119" 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/10.1159/000275541" target="_blank">Full Text</a>]
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<a id="Fitch1976" class="mim-anchor"></a>
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Fitch, N., Lindsay, J. R., Srolovitz, H.
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<strong>The temporal bone in the preauricular pit, cervical fistula, hearing loss syndrome.</strong>
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Ann. Otol. Rhinol. Laryng. 85: 268-275, 1976.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1083706/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1083706</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=1083706" 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/10.1177/000348947608500212" target="_blank">Full Text</a>]
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Fourman, P., Fourman, J.
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<strong>Hereditary deafness in family with ear-pits (fistula auris congenita).</strong>
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Brit. Med. J. 2: 1354-1356, 1955.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/13269867/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">13269867</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=13269867" 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/bmj.2.4952.1354" target="_blank">Full Text</a>]
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Gu, J. Z., Wagner, M. J., Haan, E. A., Wells, D. E.
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<strong>Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): implications for mapping and cloning of the BOR gene.</strong>
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Genomics 31: 201-206, 1996.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8824802/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8824802</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8824802" 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/10.1006/geno.1996.0032" target="_blank">Full Text</a>]
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Haan, E. A., Hull, Y. J., White, S., Cockington, R., Charlton, P., Callen, D. F.
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<strong>Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.</strong>
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Am. J. Med. Genet. 32: 490-494, 1989.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2773990/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2773990</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=2773990" 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/ajmg.1320320412" target="_blank">Full Text</a>]
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Hoskins, B. E., Cramer, C. H., II, Silvius, D., Zou, D., Raymond, R. M., Jr., Orten, D. J., Kimberling, W. J., Smith, R. J. H., Weil, D., Petit, C., Otto, E. A., Xu, P.-X., Hildebrandt, F.
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<strong>Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome.</strong>
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Am. J. Hum. Genet. 80: 800-804, 2007.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/17357085/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">17357085</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=17357085[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17357085" 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/10.1086/513322" target="_blank">Full Text</a>]
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Kalatzis, V., Abdelhak, S., Compain, S., Vincent, C., Petit, C.
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<strong>Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndrome.</strong>
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Genomics 34: 422-425, 1996.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8786145/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8786145</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8786145" 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/10.1006/geno.1996.0307" target="_blank">Full Text</a>]
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McLaurin, J. W., Kloepfer, H. W., Laguaite, J. K., Stallcup, T. A.
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<strong>Hereditary branchial anomalies and associated hearing impairment.</strong>
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Laryngoscope 76: 1277-1288, 1966.
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Melnick, M., Hodes, M. E., Nance, W. E., Yune, H., Sweeney, A.
|
|
<strong>Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.</strong>
|
|
Clin. Genet. 13: 425-442, 1978.
|
|
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|
|
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/657583/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">657583</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=657583" 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.1399-0004.1978.tb04142.x" target="_blank">Full Text</a>]
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</p>
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</div>
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</li>
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<li>
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<a id="13" class="mim-anchor"></a>
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<a id="Rowley1969" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
|
|
Rowley, P. T.
|
|
<strong>Familial hearing loss associated with branchial fistulas.</strong>
|
|
Pediatrics 44: 978-985, 1969.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/5365063/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">5365063</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=5365063" 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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</div>
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</li>
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<li>
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<a id="14" class="mim-anchor"></a>
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<a id="Spruijt2006" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Spruijt, L., Hoefsloot, L. H., van Schaijk, G. H. W. H., van Waardenburg, D., Kremer, B., Brackel, H. J. L., de Die-Smulders, C. E. M.
|
|
<strong>Identification of a novel EYA1 mutation presenting in a newborn with laryngomalacia, glossoptosis, retrognathia, and pectus excavatum. (Letter)</strong>
|
|
Am. J. Med. Genet. 140A: 1343-1345, 2006.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/16691597/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">16691597</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=16691597" 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/ajmg.a.31285" target="_blank">Full Text</a>]
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</p>
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</div>
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</li>
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<li>
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<a id="15" class="mim-anchor"></a>
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<a id="Stratakis1998" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Stratakis, C. A., Lin, J. P., Rennert, O. M.
|
|
<strong>Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).</strong>
|
|
Am. J. Med. Genet. 79: 209-214, 1998.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9788564/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9788564</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9788564" 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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</div>
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</li>
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<li>
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<a id="16" class="mim-anchor"></a>
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<a id="Vincent1997" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Vincent, C., Kalatzis, V., Abdelhak, S., Chaib, H., Compain, S., Helia, J., Vaneecloo, F.-M., Petit, C.
|
|
<strong>BOR and BO syndromes are allelic defects of EYA1.</strong>
|
|
Europ. J. Hum. Genet. 5: 242-246, 1997.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9359046/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9359046</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9359046" 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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</div>
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</li>
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<li>
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<a id="17" class="mim-anchor"></a>
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<a id="Wildervanck1962" class="mim-anchor"></a>
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<div class="">
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<p class="mim-text-font">
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Wildervanck, L. S.
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<strong>Hereditary malformations of the ear in three generations.</strong>
|
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Acta Otolaryng. 54: 553-560, 1962.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/14006981/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">14006981</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=14006981" 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/10.3109/00016486209126973" target="_blank">Full Text</a>]
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</p>
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</div>
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</li>
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</ol>
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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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<div>
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<a id="contributors" 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="mim-text-font">
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<a href="#mimCollapseContributors" role="button" data-toggle="collapse"> Contributors: </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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Victor A. McKusick - updated : 3/27/2007
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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 - reorganized : 8/2/2006<br>Cassandra L. Kniffin - updated : 8/1/2006<br>Victor A. McKusick - updated : 12/21/1998<br>Victor A. McKusick - updated : 10/16/1998
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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 : 5/1/1998
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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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carol : 02/09/2024
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</span>
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</div>
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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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carol : 02/08/2024<br>carol : 09/20/2019<br>carol : 05/08/2012<br>alopez : 3/29/2007<br>terry : 3/27/2007<br>carol : 8/2/2006<br>ckniffin : 8/1/2006<br>alopez : 1/13/2004<br>alopez : 1/13/2004<br>carol : 12/30/1998<br>terry : 12/21/1998<br>carol : 10/19/1998<br>terry : 10/16/1998<br>dholmes : 5/11/1998<br>carol : 5/2/1998<br>carol : 5/1/1998
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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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<div class="row">
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<div class="col-md-8 col-md-offset-1">
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<div>
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<div>
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<h3>
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<span class="mim-font">
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<strong>#</strong> 602588
|
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</span>
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</h3>
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</div>
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<div>
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<h3>
|
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<span class="mim-font">
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|
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BRANCHIOOTIC SYNDROME 1; BOS1
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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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<p>
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<span class="mim-font">
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<em>Alternative titles; symbols</em>
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</span>
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</p>
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</div>
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<div>
|
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<h4>
|
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<span class="mim-font">
|
|
BO SYNDROME 1<br />
|
|
BRANCHIOOTIC DYSPLASIA
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</span>
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</h4>
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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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<div>
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<p>
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<span class="mim-font">
|
|
Other entities represented in this entry:
|
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</span>
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</p>
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</div>
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<div>
|
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<span class="h3 mim-font">
|
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ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED
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</span>
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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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<div>
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<p>
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<span class="mim-text-font">
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<strong>SNOMEDCT:</strong> 764810000;
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<strong>ORPHA:</strong> 52429;
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<strong>DO:</strong> 0060232;
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</span>
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</p>
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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>Phenotype-Gene Relationships</strong>
|
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</span>
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</h4>
|
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<div>
|
|
<table class="table table-bordered table-condensed small mim-table-padding">
|
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<thead>
|
|
<tr class="active">
|
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<th>
|
|
Location
|
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</th>
|
|
<th>
|
|
Phenotype
|
|
</th>
|
|
<th>
|
|
Phenotype <br /> MIM number
|
|
</th>
|
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<th>
|
|
Inheritance
|
|
</th>
|
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<th>
|
|
Phenotype <br /> mapping key
|
|
</th>
|
|
<th>
|
|
Gene/Locus
|
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</th>
|
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<th>
|
|
Gene/Locus <br /> MIM number
|
|
</th>
|
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</tr>
|
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</thead>
|
|
<tbody>
|
|
|
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<tr>
|
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<td>
|
|
<span class="mim-font">
|
|
8q13.3
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
Anterior segment anomalies with or without cataract
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
602588
|
|
</span>
|
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</td>
|
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<td>
|
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<span class="mim-font">
|
|
Autosomal dominant
|
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</span>
|
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</td>
|
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<td>
|
|
<span class="mim-font">
|
|
3
|
|
</span>
|
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</td>
|
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<td>
|
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<span class="mim-font">
|
|
EYA1
|
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</span>
|
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</td>
|
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<td>
|
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<span class="mim-font">
|
|
601653
|
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</span>
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</td>
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</tr>
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<tr>
|
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<td>
|
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<span class="mim-font">
|
|
8q13.3
|
|
</span>
|
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</td>
|
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<td>
|
|
<span class="mim-font">
|
|
Branchiootic syndrome 1
|
|
</span>
|
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</td>
|
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<td>
|
|
<span class="mim-font">
|
|
602588
|
|
</span>
|
|
</td>
|
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<td>
|
|
<span class="mim-font">
|
|
Autosomal dominant
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
3
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
EYA1
|
|
</span>
|
|
</td>
|
|
<td>
|
|
<span class="mim-font">
|
|
601653
|
|
</span>
|
|
</td>
|
|
</tr>
|
|
|
|
</tbody>
|
|
</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>
|
|
<span class="mim-font">
|
|
<strong>TEXT</strong>
|
|
</span>
|
|
</h4>
|
|
|
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<span class="mim-text-font">
|
|
<p>A number sign (#) is used with this entry because of evidence that branchiootic syndrome-1 (BOS1) is caused by heterozygous mutation in the EYA1 gene (601653) on chromosome 8q13.</p><p>Anterior segment anomalies with or without cataract is also caused by heterozygous mutation in the EYA1 gene.</p>
|
|
</span>
|
|
<div>
|
|
<br />
|
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</div>
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<div>
|
|
<h4>
|
|
<span class="mim-font">
|
|
<strong>Description</strong>
|
|
</span>
|
|
</h4>
|
|
</div>
|
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<span class="mim-text-font">
|
|
<p>Individuals with the branchiootic syndrome (BOS) are affected by the same branchial and otic anomalies as those seen in individuals with the branchiootorenal syndrome (see BOR1, 113650), but lack renal anomalies (Vincent et al., 1997). </p><p>Although Melnick et al. (1978) maintained that the BO syndrome is distinct from the BOR syndrome because of the lack of renal anomalies and variable presence of deafness in the former, Cremers and Fikkers-van Noord (1980) suggested that the 2 syndromes represent a single entity. </p><p>See 113600 for a discussion of branchial cleft anomalies, which may be related.</p><p><strong><em>Genetic Heterogeneity of Branchiootic Syndrome</em></strong></p><p>
|
|
See also BOS2 (120502), mapped to chromosome 1, and BOS3 (608389), caused by mutation in the SIX1 gene (601205) on chromosome 14q23.</p>
|
|
</span>
|
|
<div>
|
|
<br />
|
|
</div>
|
|
|
|
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|
|
<div>
|
|
<h4>
|
|
<span class="mim-font">
|
|
<strong>Clinical Features</strong>
|
|
</span>
|
|
</h4>
|
|
</div>
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<span class="mim-text-font">
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<p>Fourman and Fourman (1955) described a large multigenerational family in which 17 members had preauricular pits, 12 of whom also had mild to severe sensorineural hearing loss. Among family members without preauricular pits, 3 had hearing loss: one of these individuals had a branchial pit. Some reported onset of hearing loss in childhood, whereas others had onset beginning at about age 20 years. Audiograms showed both high and low tone loss, usually high tone more than low. There was no evidence of vestibular disorder. The authors suggested that ear pits, deafness, and branchial fistulae were independent effects of a single dominant gene with incomplete penetrance. </p><p>Wildervanck (1962) reported a family in which 14 members had either deformed auricles, marginal pits, or preauricular appendages. Two had a moderate conductive deafness: bilateral in 1 and unilateral in the other. The mode of inheritance was dominant with full penetration. Wildervanck (1962) suggested this was a different syndrome from that described by Fourman and Fourman (1955). McLaurin et al. (1966) reported a kindred with branchial anomalies and associated hearing impairment similar to the kindred described by Wildervanck (1962). Brusis (1974) reported a kindred similar to the one described by Fourman and Fourman (1955). </p><p>Vincent et al. (1997) reported 2 families with the BO syndrome. Clinical features included branchial cervical fistulae, cup-shaped pinnae, preauricular pits, and sensorineural, conductive, or mixed hearing loss. There was no evidence of renal anomalies. </p><p>Spruijt et al. (2006) reported an infant with severe obstructive sleep apnea caused by laryngomalacia, pharyngomalacia, glossoptosis, and tracheobronchomalacia. He also had bilateral branchial fistulae and ear anomalies, including ear pits, simple helices, and slight cup-shaped and low-set left ear. The features suggested BO syndrome. Other findings included micro- and retrognathia, but kidneys and hearing were normal. Surgical intervention improved the upper airway obstruction, but mild delay and mental and motor development were observed at age 11 months. His mildly affected mother showed mild retrognathia, left-sided branchial neck fistula, left-sided preauricular pit, and right-sided branchial cyst in the neck. Kidney ultrasound and hearing were normal. Both mother and son were heterozygous for a truncating mutation in the EYA1 gene (601653.0015). Spruijt et al. (2006) emphasized the phenotypic variability of BO syndrome associated with EYA1 mutations. </p>
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<strong>Cytogenetics</strong>
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<p>Haan et al. (1989) reported a complex inherited rearrangement of chromosome 8q associated with both trichorhinophalangeal syndrome (TRPS1; 190350) and the BO syndrome in an affected Australian family showing features of both disorders. Preauricular pits or branchial sinuses were present in all 8 members studied in detail; 7 of these had deafness, the exception being the youngest. Three breakpoints in 8q were identified, resulting in dir ins(8)(q24.11q13.3q21.13). One of them was consistent with the previously assigned location of the TRPS1 locus on 8q24. Haan et al. (1989) concluded that the BO syndrome is caused by mutation at either 8q13.3 or 8q21.13. </p><p>Gu et al. (1996) made use of a cell line from one of the affected members of the family reported by Haan et al. (1989). YACs spanning the BO interval from D8S543 to D8S541 were used as fluorescence in situ hybridization probes. In addition to the cytogenetically defined direct insertion of material from 8q13.3-q21.13 into 8q24.11, a previously unidentified deletion of just under 1 megabase was found in 8q13.3. These data narrowed the most likely location of the BO gene to a region between D8S543 and D8S279. </p><p>Kalatzis et al. (1996) likewise used the cell line first described by Haan et al. (1989) and identified an associated deletion by fluorescence in situ hybridization analysis of the 8q translocation breakpoint. The generation of a YAC contig and the isolation of overlapping recombinant P1 and lambda phage clones from the region allowed further characterization of the deletion. Its size was estimated to be between 470 and 650 kb, and it was flanked by the polymorphic markers D8S1060 and D8S1807. </p>
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<strong>Mapping</strong>
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<p>Vincent et al. (1997) analyzed 2 large independent families in which each of the 8 affected members presented exclusively with BO syndrome. In both families, linkage analysis mapped the causative gene to the same region on chromosome 8q13.3. </p><p><strong><em>Genetic Heterogeneity</em></strong></p><p>
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Stratakis et al. (1998) excluded linkage to 8q13.3 in a large family with presumed autosomal dominant BO syndrome spanning 4 generations. Ear pits were present in all 15 patients, whereas hearing loss and other branchial arch anomalies were present in 40% and 20%, respectively. None of the affected members had renal abnormalities or lacrimal duct stenosis. </p>
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<strong>Molecular Genetics</strong>
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<p>Vincent et al. (1997) demonstrated a 2-bp insertion in the EYA1 gene (601653.0003) in 1 of 2 families with BO syndrome. In the other family, they detected an 8-bp deletion (601653.0004). </p><p>Spruijt et al. (2006) identified a heterozygous mutation in the EYA1 gene (601653.0014) in an infant with a variant form of BO syndrome. </p><p><strong><em>Anterior Segment Anomalies with or without Cataract</em></strong></p><p>
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Azuma et al. (2000) examined genomic DNA isolated from patients with various types of developmental eye anomalies for EYA1 mutations by use of PCR-SSCP and sequencing. They identified 3 novel missense mutations in patients who had congenital cataracts and ocular anterior segment anomalies (see, e.g., 601653.0008-601653.0009). </p>
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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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Cremers et al. (1981); Fitch et al. (1976); Hoskins et al. (2007);
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Rowley (1969)
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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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Azuma, N., Hirakiyama, A., Inoue, T., Asaka, A., Yamada, M.
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<strong>Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies.</strong>
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Hum. Molec. Genet. 9: 363-366, 2000.
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[PubMed: 10655545]
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[Full Text: https://doi.org/10.1093/hmg/9.3.363]
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Brusis, T.
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<strong>Gleichzeitiges Vorkommen von degenerativer Innenohrschwerhoerigheit, Vestibularisstoerung, beiderseitigen Ohr-und lateralen Halsfisteln bei mehreren Mitgliedern einer Familie.</strong>
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Laryng. Rhinol. Otol. 53: 131-139, 1974.
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<strong>The earpits-deafness syndrome: clinical and genetic aspects.</strong>
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Int. J. Pediat. Otorhinolaryng. 2: 309-322, 1980.
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[Full Text: https://doi.org/10.1016/0165-5876(80)90036-1]
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Cremers, C. W. R. J., Thijssen, H. O. M., Fischer, A. J. E. M., Marres, E. H. M. A.
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<strong>Otological aspects of the earpit-deafness syndrome.</strong>
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ORL 43: 223-239, 1981.
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[Full Text: https://doi.org/10.1159/000275541]
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Fitch, N., Lindsay, J. R., Srolovitz, H.
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<strong>The temporal bone in the preauricular pit, cervical fistula, hearing loss syndrome.</strong>
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Ann. Otol. Rhinol. Laryng. 85: 268-275, 1976.
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[PubMed: 1083706]
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[Full Text: https://doi.org/10.1177/000348947608500212]
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Fourman, P., Fourman, J.
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<strong>Hereditary deafness in family with ear-pits (fistula auris congenita).</strong>
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Brit. Med. J. 2: 1354-1356, 1955.
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[PubMed: 13269867]
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[Full Text: https://doi.org/10.1136/bmj.2.4952.1354]
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Gu, J. Z., Wagner, M. J., Haan, E. A., Wells, D. E.
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<strong>Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): implications for mapping and cloning of the BOR gene.</strong>
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Genomics 31: 201-206, 1996.
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[PubMed: 8824802]
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[Full Text: https://doi.org/10.1006/geno.1996.0032]
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Haan, E. A., Hull, Y. J., White, S., Cockington, R., Charlton, P., Callen, D. F.
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<strong>Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.</strong>
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Am. J. Med. Genet. 32: 490-494, 1989.
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[PubMed: 2773990]
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[Full Text: https://doi.org/10.1002/ajmg.1320320412]
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Hoskins, B. E., Cramer, C. H., II, Silvius, D., Zou, D., Raymond, R. M., Jr., Orten, D. J., Kimberling, W. J., Smith, R. J. H., Weil, D., Petit, C., Otto, E. A., Xu, P.-X., Hildebrandt, F.
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<strong>Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome.</strong>
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Am. J. Hum. Genet. 80: 800-804, 2007.
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[PubMed: 17357085]
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[Full Text: https://doi.org/10.1086/513322]
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<p class="mim-text-font">
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Kalatzis, V., Abdelhak, S., Compain, S., Vincent, C., Petit, C.
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<strong>Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndrome.</strong>
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Genomics 34: 422-425, 1996.
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[PubMed: 8786145]
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[Full Text: https://doi.org/10.1006/geno.1996.0307]
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<li>
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<p class="mim-text-font">
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McLaurin, J. W., Kloepfer, H. W., Laguaite, J. K., Stallcup, T. A.
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<strong>Hereditary branchial anomalies and associated hearing impairment.</strong>
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Laryngoscope 76: 1277-1288, 1966.
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</p>
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</li>
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<p class="mim-text-font">
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Melnick, M., Hodes, M. E., Nance, W. E., Yune, H., Sweeney, A.
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<strong>Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.</strong>
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Clin. Genet. 13: 425-442, 1978.
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[PubMed: 657583]
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[Full Text: https://doi.org/10.1111/j.1399-0004.1978.tb04142.x]
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<p class="mim-text-font">
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Rowley, P. T.
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<strong>Familial hearing loss associated with branchial fistulas.</strong>
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Pediatrics 44: 978-985, 1969.
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[PubMed: 5365063]
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Spruijt, L., Hoefsloot, L. H., van Schaijk, G. H. W. H., van Waardenburg, D., Kremer, B., Brackel, H. J. L., de Die-Smulders, C. E. M.
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<strong>Identification of a novel EYA1 mutation presenting in a newborn with laryngomalacia, glossoptosis, retrognathia, and pectus excavatum. (Letter)</strong>
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Am. J. Med. Genet. 140A: 1343-1345, 2006.
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[PubMed: 16691597]
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[Full Text: https://doi.org/10.1002/ajmg.a.31285]
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Stratakis, C. A., Lin, J. P., Rennert, O. M.
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<strong>Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).</strong>
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Am. J. Med. Genet. 79: 209-214, 1998.
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[PubMed: 9788564]
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Vincent, C., Kalatzis, V., Abdelhak, S., Chaib, H., Compain, S., Helia, J., Vaneecloo, F.-M., Petit, C.
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<strong>BOR and BO syndromes are allelic defects of EYA1.</strong>
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Europ. J. Hum. Genet. 5: 242-246, 1997.
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[PubMed: 9359046]
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Wildervanck, L. S.
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<strong>Hereditary malformations of the ear in three generations.</strong>
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Acta Otolaryng. 54: 553-560, 1962.
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[PubMed: 14006981]
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[Full Text: https://doi.org/10.3109/00016486209126973]
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Victor A. McKusick - updated : 3/27/2007<br>Cassandra L. Kniffin - reorganized : 8/2/2006<br>Cassandra L. Kniffin - updated : 8/1/2006<br>Victor A. McKusick - updated : 12/21/1998<br>Victor A. McKusick - updated : 10/16/1998
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Victor A. McKusick : 5/1/1998
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carol : 02/09/2024<br>carol : 02/08/2024<br>carol : 09/20/2019<br>carol : 05/08/2012<br>alopez : 3/29/2007<br>terry : 3/27/2007<br>carol : 8/2/2006<br>ckniffin : 8/1/2006<br>alopez : 1/13/2004<br>alopez : 1/13/2004<br>carol : 12/30/1998<br>terry : 12/21/1998<br>carol : 10/19/1998<br>terry : 10/16/1998<br>dholmes : 5/11/1998<br>carol : 5/2/1998<br>carol : 5/1/1998
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