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Entry
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- #135290 - DESMOID DISEASE, HEREDITARY; DESMD
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- OMIM
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<p>
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<span class="h4">#135290</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/135290"><strong>Clinical Synopsis</strong></a>
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<a href="#text"><strong>Text</strong></a>
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<a href="#description">Description</a>
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<a href="#clinicalFeatures">Clinical Features</a>
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<a href="#inheritance">Inheritance</a>
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<a href="#molecularGenetics">Molecular Genetics</a>
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<a href="#animalModel">Animal Model</a>
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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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<li role="presentation">
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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 style="display: table-cell;">External Links</div>
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</h4>
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<div style="display: table-cell;">Clinical Resources</div>
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<div><a href="https://clinicaltrials.gov/search?cond=DESMOID DISEASE, HEREDITARY" 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=8665&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/NBK1345/" 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/2216" 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://medlineplus.gov/genetics/condition/desmoid-tumor" class="mim-tip-hint" title="Consumer-friendly information about the effects of genetic variation on human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MedlinePlus Genetics', 'domain': 'medlineplus.gov'})">MedlinePlus Genetics</a></div>
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<div><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=135290[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=873" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></div>
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<span class="small">
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<a href="#mimAnimalModelsLinksFold" id="mimAnimalModelsLinksToggle" class="collapsed mimSingletonTriangleToggle" role="button" data-toggle="collapse" data-parent="#mimExternalLinksAccordion">
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<div style="display: table-row">
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<div id="mimAnimalModelsLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5; display: table-cell;">►</div>
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<div style="display: table-cell;">Animal Models</div>
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</div>
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</a>
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</span>
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</span>
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</div>
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<div id="mimAnimalModelsLinksFold" class="panel-collapse collapse mimLinksFold" role="tabpanel">
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<div class="panel-body small mim-panel-body">
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<div><a href="https://www.alliancegenome.org/disease/DOID:0111349" class="mim-tip-hint" title="Search Across Species; explore model organism and human comparative genomics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Alliance Genome', 'domain': 'alliancegenome.org'})">Alliance Genome</a></div>
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<div><a href="http://www.informatics.jax.org/disease/135290" class="mim-tip-hint" title="Phenotypes, alleles, and disease models from Mouse Genome Informatics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Phenotype', 'domain': 'informatics.jax.org'})">MGI Mouse Phenotype</a></div>
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<div><a href="https://wormbase.org/resources/disease/DOID:0111349" class="mim-tip-hint" title="Database of the biology and genome of Caenorhabditis elegans and related nematodes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Wormbase Disease Ontology', 'domain': 'wormbase.org'})">Wormbase Disease Ontology</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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<a id="title" class="mim-anchor"></a>
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<a id="number" class="mim-anchor"></a>
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<div class="text-right">
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<a href="#" class="mim-tip-icd" qtip_title="<strong>ICD+</strong>" qtip_text="
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<strong>ORPHA:</strong> 873<br />
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<strong>DO:</strong> 0111349<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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135290
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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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DESMOID DISEASE, HEREDITARY; DESMD
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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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FIBROMATOSIS, FAMILIAL INFILTRATIVE; FIF
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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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DESMOID TUMOR CAUSED BY SOMATIC MUTATION, 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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<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/5/369?start=-3&limit=10&highlight=369">
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5q22.2
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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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Desmoid disease, hereditary
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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/135290"> 135290 </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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<a href="/entry/611731"> 611731 </a>
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- Infiltrative fibromatosis of mesentery<br />
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- Predisposed to desmoid tumor<br /> - ? Predisposed to colon cancer<br />
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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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<p>A number sign (#) is used with this entry because of evidence that hereditary desmoid disease (DESMD) can be caused by heterozygous mutation in the APC gene (<a href="/entry/611731">611731</a>) on chromosome 5q22.</p><p>A somatic mutation in the beta-catenin gene (CTNNB1; <a href="/entry/116806">116806</a>) has been observed in a desmoid tumor derived from a patient with sporadic disease.</p>
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<p>Hereditary desmoid disease usually presents as an extraintestinal manifestation of familial adenomatous polyposis (FAP; <a href="/entry/175100">175100</a>), also known as Gardner syndrome, which is an autosomal dominant disorder caused by germline mutation in the APC gene. The desmoid tumors are usually intraabdominal and, although benign, can be locally aggressive and result in significant morbidity. Desmoid tumors can also arise sporadically (<a href="#1" class="mim-tip-reference" title="Couture, J., Mitri, A., Lagace, R., Smits, R., Berk, T., Bouchard, H.-L., Fodde, R., Alman, B., Bapat, B. <strong>A germline mutation at the extreme 3-prime end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.</strong> Clin. Genet. 57: 205-212, 2000.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10782927/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10782927</a>] [<a href="https://doi.org/10.1034/j.1399-0004.2000.570306.x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10782927">Couture et al., 2000</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10782927" 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="#5" class="mim-tip-reference" title="Maher, E. R., Morson, B., Beach, R., Hodgson, S. V. <strong>Phenotypic variation in hereditary nonpolyposis colon cancer syndrome: association with infiltrative fibromatosis (desmoid tumor).</strong> Cancer 69: 2049-2051, 1992.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1544113/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1544113</a>] [<a href="https://doi.org/10.1002/1097-0142(19920415)69:8<2049::aid-cncr2820690807>3.0.co;2-6" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="1544113">Maher et al. (1992)</a> described a mother and son with marked infiltrative fibromatosis of the mesentery of the type that had been observed as part of the Gardner syndrome. However, colonic polyps, osteomas, sebaceous cysts, and congenital hypertrophy of the retinal pigment epithelium (CHRPE) typical of Gardner syndrome were not observed. In the mother, the diagnosis of infiltrative fibromatosis of the mesentery was made at age 30. Barium enema was negative for colonic polyps. She died at 32 years of age of bowel perforation and intractable abdominal sepsis; no colonic polyps were discovered postmortem. The son was found to have an abdominal mass at age 14 years. Colonoscopic examination was negative, and other extracolonic features of Gardner syndrome were not found. Family history revealed a maternal history of nonpolyposis colon cancer syndrome and breast tumor. <a href="#5" class="mim-tip-reference" title="Maher, E. R., Morson, B., Beach, R., Hodgson, S. V. <strong>Phenotypic variation in hereditary nonpolyposis colon cancer syndrome: association with infiltrative fibromatosis (desmoid tumor).</strong> Cancer 69: 2049-2051, 1992.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1544113/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1544113</a>] [<a href="https://doi.org/10.1002/1097-0142(19920415)69:8<2049::aid-cncr2820690807>3.0.co;2-6" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="1544113">Maher et al. (1992)</a> noted that affected members of this family may have had a mutation at the APC locus that predisposed them to the development of desmoid tumor and perhaps colon cancer, but not multiple polyposis. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=1544113" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#2" class="mim-tip-reference" title="Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R. <strong>Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.</strong> Am. J. Hum. Genet. 59: 1193-1201, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940264/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940264</a>]" pmid="8940264">Eccles et al. (1996)</a> described a family in which members of 3 generations showed hereditary desmoid disease characterized by multifocal fibromatosis of the paraspinal muscles, breast, occiput, arms, lower ribs, abdominal wall, and mesentery. The authors stated that some of these locations were unusual for desmoids observed in classic FAP, which usually occur in the bowel or abdominal wall. Osteomas and epidermal cysts were also observed. One patient developed carcinoma of the head of the pancreas. None of the patients had classic colonic polyposis, but 1 had a small number (less than 50) colonic polyps and 3 had fundic gland polyps. <a href="#2" class="mim-tip-reference" title="Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R. <strong>Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.</strong> Am. J. Hum. Genet. 59: 1193-1201, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940264/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940264</a>]" pmid="8940264">Eccles et al. (1996)</a> proposed the name 'hereditary desmoid disease.' In an accompanying editorial, <a href="#4" class="mim-tip-reference" title="Lynch, H. T. <strong>Desmoid tumors: genotype-phenotype differences in familial adenomatous polyposis: a nosological dilemma. (Editorial)</strong> Am. J. Hum. Genet. 59: 1184-1185, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940262/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940262</a>]" pmid="8940262">Lynch (1996)</a> suggested that the family reported by <a href="#2" class="mim-tip-reference" title="Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R. <strong>Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.</strong> Am. J. Hum. Genet. 59: 1193-1201, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940264/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940264</a>]" pmid="8940264">Eccles et al. (1996)</a> had an attenuated form of FAP with a high predilection for the development of desmoid tumors. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=8940262+8940264" 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="#1" class="mim-tip-reference" title="Couture, J., Mitri, A., Lagace, R., Smits, R., Berk, T., Bouchard, H.-L., Fodde, R., Alman, B., Bapat, B. <strong>A germline mutation at the extreme 3-prime end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.</strong> Clin. Genet. 57: 205-212, 2000.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10782927/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10782927</a>] [<a href="https://doi.org/10.1034/j.1399-0004.2000.570306.x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10782927">Couture et al. (2000)</a> described a large French Canadian family with hereditary desmoid disease. The phenotype was characterized by the early onset of multiple desmoid tumors arising near the axial skeleton and in proximal extremities. Although the penetrance of desmoid tumors was nearly 100%, the expression of the disease was variable among the different affected relatives. The most severely affected patient died due to persistent tumor growth in the cervical spine area, while other patients had an indolent course of disease with lesions located mainly on the proximal limbs. The proband who brought the family to attention was found to have a mass in the neck region at the age of 28 years. She subsequently developed multifocal tumors in the cervical area, occiput, arms, breast, and the thoracic paraspinal area. The initial lesions on the neck and extremities were excised, but disease relapse occurred at both local and distant sites. At the age of 46 years, the patient had good functional status with minor to moderate disability. Her son developed 3 lesions on his right upper extremity at 18 years. Her daughter had 1 lesion on the upper extremity at 16 years. Many gene carriers also had cutaneous cysts. Polyposis of the colon was rarely observed in the affected individuals, and no upper gastrointestinal polyps were documented. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10782927" 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>The transmission pattern of desmoid disease in the family reported by <a href="#2" class="mim-tip-reference" title="Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R. <strong>Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.</strong> Am. J. Hum. Genet. 59: 1193-1201, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940264/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940264</a>]" pmid="8940264">Eccles et al. (1996)</a> was consistent with autosomal dominant inheritance. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8940264" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p>In affected members of the family reported by <a href="#5" class="mim-tip-reference" title="Maher, E. R., Morson, B., Beach, R., Hodgson, S. V. <strong>Phenotypic variation in hereditary nonpolyposis colon cancer syndrome: association with infiltrative fibromatosis (desmoid tumor).</strong> Cancer 69: 2049-2051, 1992.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1544113/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1544113</a>] [<a href="https://doi.org/10.1002/1097-0142(19920415)69:8<2049::aid-cncr2820690807>3.0.co;2-6" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="1544113">Maher et al. (1992)</a>, <a href="#7" class="mim-tip-reference" title="Scott, R. J., Froggatt, N. J., Trembath, R. C., Evans, D. G. R., Hodgson, S. V., Maher, E. R. <strong>Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3-prime APC gene mutation.</strong> Hum. Molec. Genet. 5: 1921-1924, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8968744/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8968744</a>] [<a href="https://doi.org/10.1093/hmg/5.12.1921" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="8968744">Scott et al. (1996)</a> identified a germline deletion in the APC gene (<a href="/entry/611731#0026">611731.0026</a>). Affected members of 2 other apparently unrelated families with desmoid tumors had the same mutation, and haplotype analysis suggested a common origin. <a href="#7" class="mim-tip-reference" title="Scott, R. J., Froggatt, N. J., Trembath, R. C., Evans, D. G. R., Hodgson, S. V., Maher, E. R. <strong>Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3-prime APC gene mutation.</strong> Hum. Molec. Genet. 5: 1921-1924, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8968744/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8968744</a>] [<a href="https://doi.org/10.1093/hmg/5.12.1921" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="8968744">Scott et al. (1996)</a> concluded that FAP and hereditary desmoid disease are allelic, and that APC mutations that truncate the APC protein distal to the beta-catenin-binding domain are associated with desmoid tumors, absence of congenital hypertrophy of the retinal pigment epithelium, and variable but attenuated polyposis expression. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=8968744+1544113" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>In affected members of a family with hereditary desmoid disease, <a href="#2" class="mim-tip-reference" title="Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R. <strong>Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.</strong> Am. J. Hum. Genet. 59: 1193-1201, 1996.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940264/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940264</a>]" pmid="8940264">Eccles et al. (1996)</a> identified a heterozygous germline mutation in the 3-prime end of exon 15 of the APC gene (<a href="/entry/611731#0025">611731.0025</a>). There was somatic loss of the wildtype APC allele within several desmoid tumors. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8940264" 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="#3" class="mim-tip-reference" title="Halling, K. C., Lazzaro, C. R., Honchel, R., Bufill, J. A., Powell, S. M., Arndt, C. A. S., Lindor, N. M. <strong>Hereditary desmoid disease in a family with a germline AluI repeat mutation of the APC gene.</strong> Hum. Hered. 49: 97-102, 1999.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10077730/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10077730</a>] [<a href="https://doi.org/10.1159/000022852" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10077730">Halling et al. (1999)</a> identified a truncating mutation in the APC gene (<a href="/entry/611731#0040">611731.0040</a>) in affected members of an Amish family with autosomal dominant desmoid disease. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10077730" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>In a large French-Canadian kindred with a hereditary desmoid disease, <a href="#1" class="mim-tip-reference" title="Couture, J., Mitri, A., Lagace, R., Smits, R., Berk, T., Bouchard, H.-L., Fodde, R., Alman, B., Bapat, B. <strong>A germline mutation at the extreme 3-prime end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.</strong> Clin. Genet. 57: 205-212, 2000.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10782927/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10782927</a>] [<a href="https://doi.org/10.1034/j.1399-0004.2000.570306.x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10782927">Couture et al. (2000)</a> identified a heterozygous mutation in the APC gene (<a href="/entry/611731#0045">611731.0045</a>). A desmoid tumor from the proband carried a somatic APC mutation (<a href="/entry/611731#0046">611731.0046</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10782927" 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>Somatic Mutations</em></strong></p><p>
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<a href="#8" class="mim-tip-reference" title="Sen-Gupta, S., Van der Luijt, R. B., Bowles, L. V., Meera Khan, P., Delhanty, J. D. A. <strong>Somatic mutation of APC gene in desmoid tumour in familial adenomatous polyposis. (Letter)</strong> Lancet 342: 552-553, 1993.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8102685/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8102685</a>] [<a href="https://doi.org/10.1016/0140-6736(93)91677-e" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="8102685">Sen-Gupta et al. (1993)</a> identified a somatic deletion in the APC gene in desmoid tissue derived from an FAP patient with a deletion at 5q. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8102685" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>In desmoid tumor tissue from a patient with sporadic disease, <a href="#9" class="mim-tip-reference" title="Shitoh, K., Konishi, F., Iijima, T., Ohdaira, T., Sakai, K., Kanazawa, K., Miyaki, M. <strong>A novel case of a sporadic desmoid tumour with mutation of the beta catenin gene.</strong> J. Clin. Path. 52: 695-696, 1999.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10655994/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10655994</a>] [<a href="https://doi.org/10.1136/jcp.52.9.695" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10655994">Shitoh et al. (1999)</a> identified a somatic mutation in the gene encoding beta-catenin (<a href="/entry/116806#0003">116806.0003</a>). The patient had no personal or family history of FAP. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10655994" 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>Cyclooxygenase-2 (COX2; <a href="/entry/600262">600262</a>) is an enzyme involved in prostaglandin synthesis that modulates the formation of colonic neoplasia, especially in cases due to mutations resulting in beta-catenin stabilization. <a href="#6" class="mim-tip-reference" title="Poon, R., Smits, R., Li, C., Jagmohan-Changur, S., Kong, M., Cheon, S., Yu, C., Fodde, R., Alman, B. A. <strong>Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor).</strong> Oncogene 20: 451-460, 2001.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/11313976/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">11313976</a>] [<a href="https://doi.org/10.1038/sj.onc.1204107" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="11313976">Poon et al. (2001)</a> found that human aggressive fibromatoses and lesions from mice heterozygous for the 1638N mutation of the Apc gene (a murine model for Apc-driven fibromatosis) demonstrated elevated COX2 levels. COX2 blockade, either by the selective agent DFU or by nonselective COX-blocking agents, resulted in reduced proliferation in human tumor cell cultures. Mice fed various COX-blocking agents showed a decline in tumor size. <a href="#6" class="mim-tip-reference" title="Poon, R., Smits, R., Li, C., Jagmohan-Changur, S., Kong, M., Cheon, S., Yu, C., Fodde, R., Alman, B. A. <strong>Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor).</strong> Oncogene 20: 451-460, 2001.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/11313976/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">11313976</a>] [<a href="https://doi.org/10.1038/sj.onc.1204107" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="11313976">Poon et al. (2001)</a> concluded that although COX blockade alone does not cause tumor regression, it may have a role as an adjuvant therapy to slow tumor growth in this lesion. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=11313976" 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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Couture, J., Mitri, A., Lagace, R., Smits, R., Berk, T., Bouchard, H.-L., Fodde, R., Alman, B., Bapat, B.
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<strong>A germline mutation at the extreme 3-prime end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.</strong>
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Clin. Genet. 57: 205-212, 2000.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10782927/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10782927</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10782927" 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/10.1034/j.1399-0004.2000.570306.x" target="_blank">Full Text</a>]
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Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R.
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<strong>Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.</strong>
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Am. J. Hum. Genet. 59: 1193-1201, 1996.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940264/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940264</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8940264" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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Halling, K. C., Lazzaro, C. R., Honchel, R., Bufill, J. A., Powell, S. M., Arndt, C. A. S., Lindor, N. M.
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<strong>Hereditary desmoid disease in a family with a germline AluI repeat mutation of the APC gene.</strong>
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Hum. Hered. 49: 97-102, 1999.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10077730/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10077730</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10077730" 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/10.1159/000022852" target="_blank">Full Text</a>]
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<strong>Desmoid tumors: genotype-phenotype differences in familial adenomatous polyposis: a nosological dilemma. (Editorial)</strong>
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Am. J. Hum. Genet. 59: 1184-1185, 1996.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8940262/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8940262</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8940262" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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Maher, E. R., Morson, B., Beach, R., Hodgson, S. V.
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<strong>Phenotypic variation in hereditary nonpolyposis colon cancer syndrome: association with infiltrative fibromatosis (desmoid tumor).</strong>
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Cancer 69: 2049-2051, 1992.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1544113/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1544113</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=1544113" 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/10.1002/1097-0142(19920415)69:8<2049::aid-cncr2820690807>3.0.co;2-6" target="_blank">Full Text</a>]
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Poon, R., Smits, R., Li, C., Jagmohan-Changur, S., Kong, M., Cheon, S., Yu, C., Fodde, R., Alman, B. A.
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<strong>Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor).</strong>
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Oncogene 20: 451-460, 2001.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/11313976/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">11313976</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=11313976" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1038/sj.onc.1204107" target="_blank">Full Text</a>]
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Scott, R. J., Froggatt, N. J., Trembath, R. C., Evans, D. G. R., Hodgson, S. V., Maher, E. R.
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<strong>Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3-prime APC gene mutation.</strong>
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Hum. Molec. Genet. 5: 1921-1924, 1996.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8968744/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8968744</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8968744" 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/5.12.1921" target="_blank">Full Text</a>]
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Sen-Gupta, S., Van der Luijt, R. B., Bowles, L. V., Meera Khan, P., Delhanty, J. D. A.
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<strong>Somatic mutation of APC gene in desmoid tumour in familial adenomatous polyposis. (Letter)</strong>
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Lancet 342: 552-553, 1993.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8102685/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8102685</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8102685" 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/10.1016/0140-6736(93)91677-e" target="_blank">Full Text</a>]
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<a id="Shitoh1999" class="mim-anchor"></a>
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Shitoh, K., Konishi, F., Iijima, T., Ohdaira, T., Sakai, K., Kanazawa, K., Miyaki, M.
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<strong>A novel case of a sporadic desmoid tumour with mutation of the beta catenin gene.</strong>
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J. Clin. Path. 52: 695-696, 1999.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10655994/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10655994</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10655994" 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/jcp.52.9.695" target="_blank">Full Text</a>]
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Cassandra L. Kniffin - updated : 1/28/2008
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Victor A. McKusick - updated : 4/9/2001<br>Victor A. McKusick - updated : 1/7/2000<br>Moyra Smith - updated : 1/24/1997
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<span class="mim-text-font">
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Victor A. McKusick : 6/22/1992
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carol : 05/08/2022
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carol : 03/20/2020<br>mgross : 11/24/2014<br>carol : 2/5/2008<br>ckniffin : 1/28/2008<br>carol : 1/16/2008<br>carol : 6/6/2001<br>terry : 4/9/2001<br>terry : 4/9/2001<br>carol : 4/2/2001<br>carol : 3/6/2001<br>terry : 1/7/2000<br>joanna : 8/12/1997<br>terry : 4/14/1997<br>mark : 1/25/1997<br>terry : 1/24/1997<br>mark : 1/24/1997<br>jamie : 1/15/1997<br>terry : 1/7/1997<br>mimadm : 9/24/1994<br>terry : 5/13/1994<br>carol : 11/1/1993<br>carol : 6/22/1992
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<strong>#</strong> 135290
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DESMOID DISEASE, HEREDITARY; DESMD
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FIBROMATOSIS, FAMILIAL INFILTRATIVE; FIF
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Other entities represented in this entry:
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DESMOID TUMOR CAUSED BY SOMATIC MUTATION, INCLUDED
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<strong>ORPHA:</strong> 873;
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<strong>DO:</strong> 0111349;
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<strong>Phenotype-Gene Relationships</strong>
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Location
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Phenotype
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Phenotype <br /> MIM number
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Inheritance
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Phenotype <br /> mapping key
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5q22.2
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Desmoid disease, hereditary
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135290
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Autosomal dominant
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<span class="mim-font">
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3
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APC
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611731
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<p>A number sign (#) is used with this entry because of evidence that hereditary desmoid disease (DESMD) can be caused by heterozygous mutation in the APC gene (611731) on chromosome 5q22.</p><p>A somatic mutation in the beta-catenin gene (CTNNB1; 116806) has been observed in a desmoid tumor derived from a patient with sporadic disease.</p>
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<strong>Description</strong>
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<p>Hereditary desmoid disease usually presents as an extraintestinal manifestation of familial adenomatous polyposis (FAP; 175100), also known as Gardner syndrome, which is an autosomal dominant disorder caused by germline mutation in the APC gene. The desmoid tumors are usually intraabdominal and, although benign, can be locally aggressive and result in significant morbidity. Desmoid tumors can also arise sporadically (Couture et al., 2000). </p>
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<p>Maher et al. (1992) described a mother and son with marked infiltrative fibromatosis of the mesentery of the type that had been observed as part of the Gardner syndrome. However, colonic polyps, osteomas, sebaceous cysts, and congenital hypertrophy of the retinal pigment epithelium (CHRPE) typical of Gardner syndrome were not observed. In the mother, the diagnosis of infiltrative fibromatosis of the mesentery was made at age 30. Barium enema was negative for colonic polyps. She died at 32 years of age of bowel perforation and intractable abdominal sepsis; no colonic polyps were discovered postmortem. The son was found to have an abdominal mass at age 14 years. Colonoscopic examination was negative, and other extracolonic features of Gardner syndrome were not found. Family history revealed a maternal history of nonpolyposis colon cancer syndrome and breast tumor. Maher et al. (1992) noted that affected members of this family may have had a mutation at the APC locus that predisposed them to the development of desmoid tumor and perhaps colon cancer, but not multiple polyposis. </p><p>Eccles et al. (1996) described a family in which members of 3 generations showed hereditary desmoid disease characterized by multifocal fibromatosis of the paraspinal muscles, breast, occiput, arms, lower ribs, abdominal wall, and mesentery. The authors stated that some of these locations were unusual for desmoids observed in classic FAP, which usually occur in the bowel or abdominal wall. Osteomas and epidermal cysts were also observed. One patient developed carcinoma of the head of the pancreas. None of the patients had classic colonic polyposis, but 1 had a small number (less than 50) colonic polyps and 3 had fundic gland polyps. Eccles et al. (1996) proposed the name 'hereditary desmoid disease.' In an accompanying editorial, Lynch (1996) suggested that the family reported by Eccles et al. (1996) had an attenuated form of FAP with a high predilection for the development of desmoid tumors. </p><p>Couture et al. (2000) described a large French Canadian family with hereditary desmoid disease. The phenotype was characterized by the early onset of multiple desmoid tumors arising near the axial skeleton and in proximal extremities. Although the penetrance of desmoid tumors was nearly 100%, the expression of the disease was variable among the different affected relatives. The most severely affected patient died due to persistent tumor growth in the cervical spine area, while other patients had an indolent course of disease with lesions located mainly on the proximal limbs. The proband who brought the family to attention was found to have a mass in the neck region at the age of 28 years. She subsequently developed multifocal tumors in the cervical area, occiput, arms, breast, and the thoracic paraspinal area. The initial lesions on the neck and extremities were excised, but disease relapse occurred at both local and distant sites. At the age of 46 years, the patient had good functional status with minor to moderate disability. Her son developed 3 lesions on his right upper extremity at 18 years. Her daughter had 1 lesion on the upper extremity at 16 years. Many gene carriers also had cutaneous cysts. Polyposis of the colon was rarely observed in the affected individuals, and no upper gastrointestinal polyps were documented. </p>
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<strong>Inheritance</strong>
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<p>The transmission pattern of desmoid disease in the family reported by Eccles et al. (1996) was consistent with autosomal dominant inheritance. </p>
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<strong>Molecular Genetics</strong>
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<p>In affected members of the family reported by Maher et al. (1992), Scott et al. (1996) identified a germline deletion in the APC gene (611731.0026). Affected members of 2 other apparently unrelated families with desmoid tumors had the same mutation, and haplotype analysis suggested a common origin. Scott et al. (1996) concluded that FAP and hereditary desmoid disease are allelic, and that APC mutations that truncate the APC protein distal to the beta-catenin-binding domain are associated with desmoid tumors, absence of congenital hypertrophy of the retinal pigment epithelium, and variable but attenuated polyposis expression. </p><p>In affected members of a family with hereditary desmoid disease, Eccles et al. (1996) identified a heterozygous germline mutation in the 3-prime end of exon 15 of the APC gene (611731.0025). There was somatic loss of the wildtype APC allele within several desmoid tumors. </p><p>Halling et al. (1999) identified a truncating mutation in the APC gene (611731.0040) in affected members of an Amish family with autosomal dominant desmoid disease. </p><p>In a large French-Canadian kindred with a hereditary desmoid disease, Couture et al. (2000) identified a heterozygous mutation in the APC gene (611731.0045). A desmoid tumor from the proband carried a somatic APC mutation (611731.0046). </p><p><strong><em>Somatic Mutations</em></strong></p><p>
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Sen-Gupta et al. (1993) identified a somatic deletion in the APC gene in desmoid tissue derived from an FAP patient with a deletion at 5q. </p><p>In desmoid tumor tissue from a patient with sporadic disease, Shitoh et al. (1999) identified a somatic mutation in the gene encoding beta-catenin (116806.0003). The patient had no personal or family history of FAP. </p>
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<strong>Animal Model</strong>
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<p>Cyclooxygenase-2 (COX2; 600262) is an enzyme involved in prostaglandin synthesis that modulates the formation of colonic neoplasia, especially in cases due to mutations resulting in beta-catenin stabilization. Poon et al. (2001) found that human aggressive fibromatoses and lesions from mice heterozygous for the 1638N mutation of the Apc gene (a murine model for Apc-driven fibromatosis) demonstrated elevated COX2 levels. COX2 blockade, either by the selective agent DFU or by nonselective COX-blocking agents, resulted in reduced proliferation in human tumor cell cultures. Mice fed various COX-blocking agents showed a decline in tumor size. Poon et al. (2001) concluded that although COX blockade alone does not cause tumor regression, it may have a role as an adjuvant therapy to slow tumor growth in this lesion. </p>
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<strong>REFERENCES</strong>
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</h4>
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<div>
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<p />
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Couture, J., Mitri, A., Lagace, R., Smits, R., Berk, T., Bouchard, H.-L., Fodde, R., Alman, B., Bapat, B.
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<strong>A germline mutation at the extreme 3-prime end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.</strong>
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Clin. Genet. 57: 205-212, 2000.
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[PubMed: 10782927]
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[Full Text: https://doi.org/10.1034/j.1399-0004.2000.570306.x]
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</p>
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<p class="mim-text-font">
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Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R.
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<strong>Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.</strong>
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Am. J. Hum. Genet. 59: 1193-1201, 1996.
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[PubMed: 8940264]
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Halling, K. C., Lazzaro, C. R., Honchel, R., Bufill, J. A., Powell, S. M., Arndt, C. A. S., Lindor, N. M.
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<strong>Hereditary desmoid disease in a family with a germline AluI repeat mutation of the APC gene.</strong>
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Lynch, H. T.
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Maher, E. R., Morson, B., Beach, R., Hodgson, S. V.
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<strong>Phenotypic variation in hereditary nonpolyposis colon cancer syndrome: association with infiltrative fibromatosis (desmoid tumor).</strong>
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Cancer 69: 2049-2051, 1992.
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[Full Text: https://doi.org/10.1002/1097-0142(19920415)69:8<2049::aid-cncr2820690807>3.0.co;2-6]
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Poon, R., Smits, R., Li, C., Jagmohan-Changur, S., Kong, M., Cheon, S., Yu, C., Fodde, R., Alman, B. A.
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<strong>Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor).</strong>
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Scott, R. J., Froggatt, N. J., Trembath, R. C., Evans, D. G. R., Hodgson, S. V., Maher, E. R.
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<strong>Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3-prime APC gene mutation.</strong>
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Sen-Gupta, S., Van der Luijt, R. B., Bowles, L. V., Meera Khan, P., Delhanty, J. D. A.
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<strong>Somatic mutation of APC gene in desmoid tumour in familial adenomatous polyposis. (Letter)</strong>
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Shitoh, K., Konishi, F., Iijima, T., Ohdaira, T., Sakai, K., Kanazawa, K., Miyaki, M.
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<strong>A novel case of a sporadic desmoid tumour with mutation of the beta catenin gene.</strong>
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Cassandra L. Kniffin - updated : 1/28/2008<br>Victor A. McKusick - updated : 4/9/2001<br>Victor A. McKusick - updated : 1/7/2000<br>Moyra Smith - updated : 1/24/1997
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Victor A. McKusick : 6/22/1992
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