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<meta name="keywords" content="C5830355, deafness, autosomal dominant 88, dfna88, disease or syndrome, epha10, hearing loss, autosomal dominant 88, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="Autosomal dominant deafness-88 (DFNA88) is characterized by nonsyndromic postlingual progressive severe sensorineural hearing loss with tinnitus (Jiang et al., 2011; Huang et al., 2023)." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Hearing loss, autosomal dominant 88 (Concept Id: C5830355)
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<!--
UID=1840991
ConceptID=C5830355
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Hearing loss, autosomal dominant 88<span class="h1sub">(DFNA88)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1840991</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information."><span class="highlight" style="background-color:">C5830355</span></a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
<td>Deafness, autosomal dominant 88</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Gene (location):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
Gene(s) directly associated with<br />
this condition or phenotype.</div></td>
<td><a target="_blank" title="EPHA10 - ID: 284656 - NCBI Gene" href="/gene/284656" class="medgenPMinfo">EPHA10</a> (1p34.3)</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
<td><a href="https://monarchinitiative.org/disease/MONDO:0859527" target="_blank">MONDO:0859527</a></td></tr>
<tr><td>OMIM<span class="superscript">®</span>:</td>
<td><a href="https://omim.org/entry/620283" target="_blank">620283</a></td></tr>
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
<div class="portlet mgSection" id="ID_100">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">Autosomal dominant deafness-88 (DFNA88) is characterized by nonsyndromic postlingual progressive severe sensorineural hearing loss with tinnitus (Jiang et al., 2011; Huang et al., 2023). [from <a title="Online Mendelian Inheritance in Man" href="http://www.omim.org" class="defSource" target="_blank">OMIM</a>]</div>
</div>
<div class="portlet mgSection" id="ID_102">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
<div class="divPopper rprt" id="clin_235586"><div><strong>Hearing impairment</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>235586</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C1384666</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">A decreased magnitude of the sensory perception of sound.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/235586">Feature record</a> | <a href="/medgen?term=%22Hearing%20impairment%22%5BClinical%20Features%5D%20OR%20235586%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite"><ul><li><span class="TLline">Ear malformation</span><ul><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_235586" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hearing impairment</a></span></li></ul></li></ul></div></div>
</div>
<div class="portlet mgSection" id="ID_105">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
<div class="nl"><a target="_blank" href="/pubmed/38445406">Genotype-Phenotype correlation of distal renal tubular acidosis in Tunisia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hammi Y,
Charfi H,
Ferjani M,
Sayari T,
Mrad R,
Gargah T</span><br />
<span class="medgenPMjournal">Tunis Med</span>
2023 Aug-Sep;101(8-9):704-708.
<span class="bold">PMID: </span><a href="/pubmed/38445406" target="_blank">38445406</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(hearing%20loss%2C%20autosomal%20dominant%2088)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (1)</a></div></div>
</div>
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
<div class="portlet mgSection" id="ID_103">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
<div class="nl"><a target="_blank" href="/pubmed/38445406">Genotype-Phenotype correlation of distal renal tubular acidosis in Tunisia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hammi Y,
Charfi H,
Ferjani M,
Sayari T,
Mrad R,
Gargah T</span><br />
<span class="medgenPMjournal">Tunis Med</span>
2023 Aug-Sep;101(8-9):704-708.
<span class="bold">PMID: </span><a href="/pubmed/38445406" target="_blank">38445406</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12745286">Sebastian syndrome: report of the first case in a South American family.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Balderramo DC,
Ricchi BN,
Marun SG,
Scaliter G,
Alonso M</span><br />
<span class="medgenPMjournal">Haematologica</span>
2003 May;88(5):ECR17.
<span class="bold">PMID: </span><a href="/pubmed/12745286" target="_blank">12745286</a></div>
<div class="nl"><a target="_blank" href="/pubmed/10769282">Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schönberger J,
Levy H,
Grünig E,
Sangwatanaroj S,
Fatkin D,
MacRae C,
Stäcker H,
Halpin C,
Eavey R,
Philbin EF,
Katus H,
Seidman JG,
Seidman CE</span><br />
<span class="medgenPMjournal">Circulation</span>
2000 Apr 18;101(15):1812-8.
doi: 10.1161/01.cir.101.15.1812.
<span class="bold">PMID: </span><a href="/pubmed/10769282" target="_blank">10769282</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hearing%20loss%2C%20autosomal%20dominant%2088%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (3)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/37847107">Clinical Variability in a Family with Noonan Syndrome with a Homozygous PTPN11 Gene Variant in Two Individuals.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yıldırım R,
Unal E,
Özalkak Ş,
Akalın A,
Aykut A,
Yılmaz N</span><br />
<span class="medgenPMjournal">J Clin Res Pediatr Endocrinol</span>
2024 Mar 11;16(1):76-83.
Epub 2023 Oct 17
doi: 10.4274/jcrpe.galenos.2023.2023-5-16.
<span class="bold">PMID: </span><a href="/pubmed/37847107" target="_blank">37847107</a><a href="/pmc/articles/PMC10938517" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/38445406">Genotype-Phenotype correlation of distal renal tubular acidosis in Tunisia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hammi Y,
Charfi H,
Ferjani M,
Sayari T,
Mrad R,
Gargah T</span><br />
<span class="medgenPMjournal">Tunis Med</span>
2023 Aug-Sep;101(8-9):704-708.
<span class="bold">PMID: </span><a href="/pubmed/38445406" target="_blank">38445406</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33111345">Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Brownstein Z,
Gulsuner S,
Walsh T,
Martins FTA,
Taiber S,
Isakov O,
Lee MK,
Bordeynik-Cohen M,
Birkan M,
Chang W,
Casadei S,
Danial-Farran N,
Abu-Rayyan A,
Carlson R,
Kamal L,
Arnthórsson AÖ,
Sokolov M,
Gilony D,
Lipschitz N,
Frydman M,
Davidov B,
Macarov M,
Sagi M,
Vinkler C,
Poran H,
Sharony R,
Samra N,
Zvi N,
Baris-Feldman H,
Singer A,
Handzel O,
Hertzano R,
Ali-Naffaa D,
Ruhrman-Shahar N,
Madgar O,
Sofrin-Drucker E,
Peleg A,
Khayat M,
Shohat M,
Basel-Salmon L,
Pras E,
Lev D,
Wolf M,
Steingrimsson E,
Shomron N,
Kelley MW,
Kanaan MN,
Allon-Shalev S,
King MC,
Avraham KB</span><br />
<span class="medgenPMjournal">Clin Genet</span>
2020 Oct;98(4):353-364.
Epub 2020 Aug 24
doi: 10.1111/cge.13817.
<span class="bold">PMID: </span><a href="/pubmed/33111345" target="_blank">33111345</a><a href="/pmc/articles/PMC8045518" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29287889">A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cesca F,
Bettella E,
Polli R,
Cama E,
Scimemi P,
Santarelli R,
Murgia A</span><br />
<span class="medgenPMjournal">Int J Pediatr Otorhinolaryngol</span>
2018 Jan;104:88-93.
Epub 2017 Oct 31
doi: 10.1016/j.ijporl.2017.10.042.
<span class="bold">PMID: </span><a href="/pubmed/29287889" target="_blank">29287889</a></div>
<div class="nl"><a target="_blank" href="/pubmed/24890873">R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Verver E,
Pecci A,
De Rocco D,
Ryhänen S,
Barozzi S,
Kunst H,
Topsakal V,
Savoia A</span><br />
<span class="medgenPMjournal">Clin Genet</span>
2015 Jul;88(1):85-9.
Epub 2014 Jul 26
doi: 10.1111/cge.12438.
<span class="bold">PMID: </span><a href="/pubmed/24890873" target="_blank">24890873</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hearing%20loss%2C%20autosomal%20dominant%2088%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (7)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/15113126">High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Minárik G,
Ferák V,
Feráková E,
Ficek A,
Poláková H,
Kádasi L</span><br />
<span class="medgenPMjournal">Gen Physiol Biophys</span>
2003 Dec;22(4):549-56.
<span class="bold">PMID: </span><a href="/pubmed/15113126" target="_blank">15113126</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hearing%20loss%2C%20autosomal%20dominant%2088%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/29287889">A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cesca F,
Bettella E,
Polli R,
Cama E,
Scimemi P,
Santarelli R,
Murgia A</span><br />
<span class="medgenPMjournal">Int J Pediatr Otorhinolaryngol</span>
2018 Jan;104:88-93.
Epub 2017 Oct 31
doi: 10.1016/j.ijporl.2017.10.042.
<span class="bold">PMID: </span><a href="/pubmed/29287889" target="_blank">29287889</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hearing%20loss%2C%20autosomal%20dominant%2088%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/37847107">Clinical Variability in a Family with Noonan Syndrome with a Homozygous PTPN11 Gene Variant in Two Individuals.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yıldırım R,
Unal E,
Özalkak Ş,
Akalın A,
Aykut A,
Yılmaz N</span><br />
<span class="medgenPMjournal">J Clin Res Pediatr Endocrinol</span>
2024 Mar 11;16(1):76-83.
Epub 2023 Oct 17
doi: 10.4274/jcrpe.galenos.2023.2023-5-16.
<span class="bold">PMID: </span><a href="/pubmed/37847107" target="_blank">37847107</a><a href="/pmc/articles/PMC10938517" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29287889">A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cesca F,
Bettella E,
Polli R,
Cama E,
Scimemi P,
Santarelli R,
Murgia A</span><br />
<span class="medgenPMjournal">Int J Pediatr Otorhinolaryngol</span>
2018 Jan;104:88-93.
Epub 2017 Oct 31
doi: 10.1016/j.ijporl.2017.10.042.
<span class="bold">PMID: </span><a href="/pubmed/29287889" target="_blank">29287889</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12522684">A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Xia J,
Deng H,
Feng Y,
Zhang H,
Pan Q,
Dai H,
Long Z,
Tang B,
Deng H,
Chen Y,
Zhang R,
Zheng D,
He Y,
Xia K</span><br />
<span class="medgenPMjournal">J Hum Genet</span>
2002;47(12):635-40.
doi: 10.1007/s100380200098.
<span class="bold">PMID: </span><a href="/pubmed/12522684" target="_blank">12522684</a></div>
<div class="nl"><a target="_blank" href="/pubmed/10769282">Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schönberger J,
Levy H,
Grünig E,
Sangwatanaroj S,
Fatkin D,
MacRae C,
Stäcker H,
Halpin C,
Eavey R,
Philbin EF,
Katus H,
Seidman JG,
Seidman CE</span><br />
<span class="medgenPMjournal">Circulation</span>
2000 Apr 18;101(15):1812-8.
doi: 10.1161/01.cir.101.15.1812.
<span class="bold">PMID: </span><a href="/pubmed/10769282" target="_blank">10769282</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hearing%20loss%2C%20autosomal%20dominant%2088%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4)</a></div></div>
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<div class="nl"><a target="_blank" href="/pubmed/38970134">A systematic review on the contribution of DNA methylation to hearing loss.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Patil V,
Perez-Carpena P,
Lopez-Escamez JA</span><br />
<span class="medgenPMjournal">Clin Epigenetics</span>
2024 Jul 5;16(1):88.
doi: 10.1186/s13148-024-01697-9.
<span class="bold">PMID: </span><a href="/pubmed/38970134" target="_blank">38970134</a><a href="/pmc/articles/PMC11227199" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hearing%20loss%2C%20autosomal%20dominant%2088%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/search?index=entry&amp;start=1&amp;limit=10&amp;sort=score%20desc&amp;field=number&amp;search=620283" target="_blank">OMIM</a></li><li><a href="https://clinicaltrials.gov/search?cond=Hearing%20loss,%20autosomal%20dominant%2088" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(hearing%20loss%2C%20autosomal%20dominant%2088)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://www.malacards.org/card/deafness_autosomal_dominant_88" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&amp;query=Hearing%20loss,%20autosomal%20dominant%2088" target="_blank">MedlinePlus</a></li></ul></div>
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