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<meta name="keywords" content="C0011053, deafness, finding, loss of hearing, 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="An inherited or acquired condition characterized by the inability to hear in one or both ears." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
UID=4155
ConceptID=C0011053
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Deafness</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>4155</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.">C0011053</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
<td>Loss of hearing</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">An inherited or acquired condition characterized by the inability to hear in one or both ears. [from <a title="NCI Thesaurus" href="http://ncit.nci.nih.gov" class="defSource" target="_blank">NCI</a>]</div>
</div>
<div class="portlet mgSection" id="ID_118">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test,  </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test,  </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM,  </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>,  </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar  </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0011053[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=4155">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=4155" ref="ncbi_uid=4155">V</a></span></span><span class="TLline">Deafness</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/75618" ref="tree=MeSH" title="MedGen record for Ear malformation">Ear malformation</a></span><ul><li><span class="TLline"><a href="/medgen/1631982" ref="tree=MeSH" title="MedGen record for Abnormal ear physiology">Abnormal ear physiology</a></span><ul><li><span class="TLline"><a href="/medgen/871365" ref="tree=MeSH" title="MedGen record for Hearing abnormality">Hearing abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/235586" ref="tree=MeSH" title="MedGen record for Hearing impairment">Hearing impairment</a></span><ul><li><span class="matched_ds">Deafness</span><ul><li><span class="TLline"><a href="/medgen/376173" ref="tree=MeSH" title="MedGen record for Autosomal dominant nonsyndromic hearing loss 36">Autosomal dominant nonsyndromic hearing loss 36</a></span></li><li><span class="TLline"><a href="/medgen/330834" ref="tree=MeSH" title="MedGen record for Autosomal dominant nonsyndromic hearing loss 41">Autosomal dominant nonsyndromic hearing loss 41</a></span></li><li><span class="TLline"><a href="/medgen/761234" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 4">Autosomal recessive nonsyndromic hearing loss 4</a></span></li><li><span class="TLline"><a href="/medgen/342839" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 28">Autosomal recessive nonsyndromic hearing loss 28</a></span></li><li><span class="TLline"><a href="/medgen/374909" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 39">Autosomal recessive nonsyndromic hearing loss 39</a></span></li><li><span class="TLline"><a href="/medgen/346670" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 49">Autosomal recessive nonsyndromic hearing loss 49</a></span></li><li><span class="TLline"><a href="/medgen/777106" ref="tree=MeSH" title="MedGen record for Bilateral deafness">Bilateral deafness</a></span></li><li><span class="TLline"><a href="/medgen/108418" ref="tree=MeSH" title="MedGen record for Complete deafness">Complete deafness</a></span></li><li><span class="TLline"><a href="/medgen/408188" ref="tree=MeSH" title="MedGen record for Deaf-Blind Disorders">Deaf-Blind Disorders</a></span><ul><li><span class="TLline"><a href="/medgen/78754" ref="tree=MeSH" title="MedGen record for Usher syndrome">Usher syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/292820" ref="tree=MeSH" title="MedGen record for Usher syndrome type 1">Usher syndrome type 1</a></span></li><li><span class="TLline"><a href="/medgen/83288" ref="tree=MeSH" title="MedGen record for Usher syndrome type 2">Usher syndrome type 2</a></span></li><li><span class="TLline"><a href="/medgen/339336" ref="tree=MeSH" title="MedGen record for Usher syndrome type 3">Usher syndrome type 3</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/21923" ref="tree=MeSH" title="MedGen record for Wolfram syndrome">Wolfram syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/1641635" ref="tree=MeSH" title="MedGen record for Wolfram syndrome 1">Wolfram syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/347604" ref="tree=MeSH" title="MedGen record for Wolfram syndrome 2">Wolfram syndrome 2</a></span></li><li><span class="TLline"><a href="/medgen/325511" ref="tree=MeSH" title="MedGen record for Wolfram syndrome, mitochondrial form">Wolfram syndrome, mitochondrial form</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/1793876" ref="tree=MeSH" title="MedGen record for Deafness due to Connexin 26 Gene Anomaly">Deafness due to Connexin 26 Gene Anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/388720" ref="tree=MeSH" title="MedGen record for Autosomal recessive nonsyndromic hearing loss 1A">Autosomal recessive nonsyndromic hearing loss 1A</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/501251" ref="tree=MeSH" title="MedGen record for Deafness, Autosomal Recessive 36">Deafness, Autosomal Recessive 36</a></span></li><li><span class="TLline"><a href="/medgen/335096" ref="tree=MeSH" title="MedGen record for Deafness, X-linked 5">Deafness, X-linked 5</a></span></li><li><span class="TLline"><a href="/medgen/376307" ref="tree=MeSH" title="MedGen record for Hearing loss, X-linked 4">Hearing loss, X-linked 4</a></span></li><li><span class="TLline"><a href="/medgen/1651816" ref="tree=MeSH" title="MedGen record for Mitochondrially Inherited Nonsyndromic Sensorineural Deafness">Mitochondrially Inherited Nonsyndromic Sensorineural Deafness</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></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/32712016">Alport Syndrome: Achieving Early Diagnosis and Treatment.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kashtan CE</span><br />
<span class="medgenPMjournal">Am J Kidney Dis</span>
2021 Feb;77(2):272-279.
Epub 2020 Jul 22
doi: 10.1053/j.ajkd.2020.03.026.
<span class="bold">PMID: </span><a href="/pubmed/32712016" target="_blank">32712016</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30093087">Update on consensus on diagnosis and treatment of idiopathic sudden sensorineural hearing loss.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Herrera M,
García Berrocal JR,
García Arumí A,
Lavilla MJ,
Plaza G;
Grupo de Trabajo de la Comisión de Audiología de la SEORL</span><br />
<span class="medgenPMjournal">Acta Otorrinolaringol Esp (Engl Ed)</span>
2019 Sep-Oct;70(5):290-300.
Epub 2018 Aug 6
doi: 10.1016/j.otorri.2018.04.010.
<span class="bold">PMID: </span><a href="/pubmed/30093087" target="_blank">30093087</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26742931">Wolfram Syndrome: Diagnosis, Management, and Treatment.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Urano F</span><br />
<span class="medgenPMjournal">Curr Diab Rep</span>
2016 Jan;16(1):6.
doi: 10.1007/s11892-015-0702-6.
<span class="bold">PMID: </span><a href="/pubmed/26742931" target="_blank">26742931</a><a href="/pmc/articles/PMC4705145" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22deafness%22%5Btiab%3A~0%5D)%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 (637)</a></div></div>
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<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/38528140">Gene therapy for deafness: are we there now?</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Moser T,
Chen H,
Kusch K,
Behr R,
Vona B</span><br />
<span class="medgenPMjournal">EMBO Mol Med</span>
2024 Apr;16(4):675-677.
Epub 2024 Mar 25
doi: 10.1038/s44321-024-00058-6.
<span class="bold">PMID: </span><a href="/pubmed/38528140" target="_blank">38528140</a><a href="/pmc/articles/PMC11018804" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31422974">Older Persons With Subjectively Assessed Hearing Problems in Poland: Quality of Life and Coping Strategies.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Domagała-Zyśk E</span><br />
<span class="medgenPMjournal">Am Ann Deaf</span>
2019;164(3):381-394.
doi: 10.1353/aad.2019.0020.
<span class="bold">PMID: </span><a href="/pubmed/31422974" target="_blank">31422974</a></div>
<div class="nl"><a target="_blank" href="/pubmed/24533753">History of cochlear implantation.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Ramsden RT</span><br />
<span class="medgenPMjournal">Cochlear Implants Int</span>
2013 Nov;14 Suppl 4:S3-5.
doi: 10.1179/1467010013Z.000000000140.
<span class="bold">PMID: </span><a href="/pubmed/24533753" target="_blank">24533753</a></div>
<div class="nl"><a target="_blank" href="/pubmed/21542710">Cochlear implants: current status and future potential.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cosetti MK,
Waltzman SB</span><br />
<span class="medgenPMjournal">Expert Rev Med Devices</span>
2011 May;8(3):389-401.
doi: 10.1586/erd.11.12.
<span class="bold">PMID: </span><a href="/pubmed/21542710" target="_blank">21542710</a></div>
<div class="nl"><a target="_blank" href="/pubmed/9351300">Pedophilia and deafness.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vernon M,
Rich S</span><br />
<span class="medgenPMjournal">Am Ann Deaf</span>
1997 Oct;142(4):300-11.
doi: 10.1353/aad.2012.0258.
<span class="bold">PMID: </span><a href="/pubmed/9351300" target="_blank">9351300</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Deafness%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 (9236)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/36444857">Keratitis-ichthyosis-deafness syndrome: A comprehensive review of cutaneous and systemic manifestations.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Alsabbagh MM</span><br />
<span class="medgenPMjournal">Pediatr Dermatol</span>
2023 Jan;40(1):19-27.
Epub 2022 Nov 29
doi: 10.1111/pde.15201.
<span class="bold">PMID: </span><a href="/pubmed/36444857" target="_blank">36444857</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26375234">Syndrome in Question.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Peruzzo J,
Nazar FL,
Tubone MQ,
Escobar GF,
Cestari TF</span><br />
<span class="medgenPMjournal">An Bras Dermatol</span>
2015 Jul-Aug;90(4):589-90.
doi: 10.1590/abd1806-4841.20153343.
<span class="bold">PMID: </span><a href="/pubmed/26375234" target="_blank">26375234</a><a href="/pmc/articles/PMC4560554" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/8493181">Hearing disorders.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Rapin I</span><br />
<span class="medgenPMjournal">Pediatr Rev</span>
1993 Feb;14(2):43-9.
doi: 10.1542/pir.14-2-43.
<span class="bold">PMID: </span><a href="/pubmed/8493181" target="_blank">8493181</a></div>
<div class="nl"><a target="_blank" href="/pubmed/2198446">Deafness: diagnosis and management.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tonkin JP</span><br />
<span class="medgenPMjournal">Med J Aust</span>
1990 Jun 18;152(12):659-63.
doi: 10.5694/j.1326-5377.1990.tb125426.x.
<span class="bold">PMID: </span><a href="/pubmed/2198446" target="_blank">2198446</a></div>
<div class="nl"><a target="_blank" href="/pubmed/5923001">Pseudohypacusis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Goldstein R</span><br />
<span class="medgenPMjournal">J Speech Hear Disord</span>
1966 Nov;31(4):341-52.
doi: 10.1044/jshd.3104.341.
<span class="bold">PMID: </span><a href="/pubmed/5923001" target="_blank">5923001</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Deafness%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 (8957)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/38280389">AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lv J,
Wang H,
Cheng X,
Chen Y,
Wang D,
Zhang L,
Cao Q,
Tang H,
Hu S,
Gao K,
Xun M,
Wang J,
Wang Z,
Zhu B,
Cui C,
Gao Z,
Guo L,
Yu S,
Jiang L,
Yin Y,
Zhang J,
Chen B,
Wang W,
Chai R,
Chen ZY,
Li H,
Shu Y</span><br />
<span class="medgenPMjournal">Lancet</span>
2024 May 25;403(10441):2317-2325.
Epub 2024 Jan 24
doi: 10.1016/S0140-6736(23)02874-X.
<span class="bold">PMID: </span><a href="/pubmed/38280389" target="_blank">38280389</a></div>
<div class="nl"><a target="_blank" href="/pubmed/38189623">AAV-Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Qi J,
Tan F,
Zhang L,
Lu L,
Zhang S,
Zhai Y,
Lu Y,
Qian X,
Dong W,
Zhou Y,
Zhang Z,
Yang X,
Jiang L,
Yu C,
Liu J,
Chen T,
Wu L,
Tan C,
Sun S,
Song H,
Shu Y,
Xu L,
Gao X,
Li H,
Chai R</span><br />
<span class="medgenPMjournal">Adv Sci (Weinh)</span>
2024 Mar;11(11):e2306788.
Epub 2024 Jan 8
doi: 10.1002/advs.202306788.
<span class="bold">PMID: </span><a href="/pubmed/38189623" target="_blank">38189623</a><a href="/pmc/articles/PMC10953563" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33979487">Tympanostomy Tubes or Medical Management for Recurrent Acute Otitis Media.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hoberman A,
Preciado D,
Paradise JL,
Chi DH,
Haralam M,
Block SL,
Kearney DH,
Bhatnagar S,
Muñiz Pujalt GB,
Shope TR,
Martin JM,
Felten DE,
Kurs-Lasky M,
Liu H,
Yahner K,
Jeong JH,
Cohen NL,
Czervionke B,
Nagg JP,
Dohar JE,
Shaikh N</span><br />
<span class="medgenPMjournal">N Engl J Med</span>
2021 May 13;384(19):1789-1799.
doi: 10.1056/NEJMoa2027278.
<span class="bold">PMID: </span><a href="/pubmed/33979487" target="_blank">33979487</a><a href="/pmc/articles/PMC8969083" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32657896">Wilson disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Aggarwal A,
Bhatt M</span><br />
<span class="medgenPMjournal">Curr Opin Neurol</span>
2020 Aug;33(4):534-542.
doi: 10.1097/WCO.0000000000000837.
<span class="bold">PMID: </span><a href="/pubmed/32657896" target="_blank">32657896</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31227837">Gene therapy for hearing loss.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Omichi R,
Shibata SB,
Morton CC,
Smith RJH</span><br />
<span class="medgenPMjournal">Hum Mol Genet</span>
2019 Oct 1;28(R1):R65-R79.
doi: 10.1093/hmg/ddz129.
<span class="bold">PMID: </span><a href="/pubmed/31227837" target="_blank">31227837</a><a href="/pmc/articles/PMC6796998" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Deafness%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 (3753)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/38069086">Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Sakata A,
Kashio A,
Koyama M,
Urata S,
Koyama H,
Yamasoba T</span><br />
<span class="medgenPMjournal">Int J Mol Sci</span>
2023 Nov 25;24(23)
doi: 10.3390/ijms242316763.
<span class="bold">PMID: </span><a href="/pubmed/38069086" target="_blank">38069086</a><a href="/pmc/articles/PMC10705933" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34333001">Hearing loss in inherited metabolic disorders: A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Trinh TT,
Blasco H,
Maillot F,
Bakhos D</span><br />
<span class="medgenPMjournal">Metabolism</span>
2021 Sep;122:154841.
Epub 2021 Jul 30
doi: 10.1016/j.metabol.2021.154841.
<span class="bold">PMID: </span><a href="/pubmed/34333001" target="_blank">34333001</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28806332">Linking Deafness and Dementia: Challenges and Opportunities.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lin VYW,
Black SE</span><br />
<span class="medgenPMjournal">Otol Neurotol</span>
2017 Sep;38(8):e237-e239.
doi: 10.1097/MAO.0000000000001408.
<span class="bold">PMID: </span><a href="/pubmed/28806332" target="_blank">28806332</a></div>
<div class="nl"><a target="_blank" href="/pubmed/9654946">The long QT syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Ackerman MJ</span><br />
<span class="medgenPMjournal">Pediatr Rev</span>
1998 Jul;19(7):232-8.
doi: 10.1542/pir.19-7-232.
<span class="bold">PMID: </span><a href="/pubmed/9654946" target="_blank">9654946</a></div>
<div class="nl"><a target="_blank" href="/pubmed/8472085">Acoustic schwannoma.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Chandler CL,
Ramsden RT</span><br />
<span class="medgenPMjournal">Br J Hosp Med</span>
1993 Mar 3-16;49(5):335-43.
<span class="bold">PMID: </span><a href="/pubmed/8472085" target="_blank">8472085</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Deafness%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 (4676)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/36928321">Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Salame M,
Bonnet C,
Moctar ECM,
Brahim SM,
Dedy A,
Vetah LA,
Veten F,
Hamed CT,
Petit C,
Houmeida A</span><br />
<span class="medgenPMjournal">Eur Arch Otorhinolaryngol</span>
2023 Sep;280(9):4057-4063.
Epub 2023 Mar 16
doi: 10.1007/s00405-023-07907-z.
<span class="bold">PMID: </span><a href="/pubmed/36928321" target="_blank">36928321</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30809665">Cued Speech Enhances Speech-in-Noise Perception.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bayard C,
Machart L,
Strauß A,
Gerber S,
Aubanel V,
Schwartz JL</span><br />
<span class="medgenPMjournal">J Deaf Stud Deaf Educ</span>
2019 Jul 1;24(3):223-233.
doi: 10.1093/deafed/enz003.
<span class="bold">PMID: </span><a href="/pubmed/30809665" target="_blank">30809665</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30033435">A Breast Cancer Education Program for D/deaf Women.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cumberland WG,
Berman BA,
Zazove P,
Sadler GR,
Jo A,
Booth H,
Wolfson A,
Stern C,
Kaufman G,
Bastani R</span><br />
<span class="medgenPMjournal">Am Ann Deaf</span>
2018;163(2):90-115.
doi: 10.1353/aad.2018.0014.
<span class="bold">PMID: </span><a href="/pubmed/30033435" target="_blank">30033435</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29551517">Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kashtan CE,
Ding J,
Garosi G,
Heidet L,
Massella L,
Nakanishi K,
Nozu K,
Renieri A,
Rheault M,
Wang F,
Gross O</span><br />
<span class="medgenPMjournal">Kidney Int</span>
2018 May;93(5):1045-1051.
Epub 2018 Mar 16
doi: 10.1016/j.kint.2017.12.018.
<span class="bold">PMID: </span><a href="/pubmed/29551517" target="_blank">29551517</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28132726">Cochlear implantation for single-sided deafness and tinnitus suppression.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Holder JT,
O'Connell B,
Hedley-Williams A,
Wanna G</span><br />
<span class="medgenPMjournal">Am J Otolaryngol</span>
2017 Mar-Apr;38(2):226-229.
Epub 2017 Jan 19
doi: 10.1016/j.amjoto.2017.01.020.
<span class="bold">PMID: </span><a href="/pubmed/28132726" target="_blank">28132726</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Deafness%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 (6905)</a></div></div>
</div>
<div class="portlet mgSection" id="ID_104">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">
<div class="nl"><a target="_blank" href="/pubmed/37963634">Autism intervention meta-analysis of early childhood studies (Project AIM): updated systematic review and secondary analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Sandbank M,
Bottema-Beutel K,
Crowley LaPoint S,
Feldman JI,
Barrett DJ,
Caldwell N,
Dunham K,
Crank J,
Albarran S,
Woynaroski T</span><br />
<span class="medgenPMjournal">BMJ</span>
2023 Nov 14;383:e076733.
doi: 10.1136/bmj-2023-076733.
<span class="bold">PMID: </span><a href="/pubmed/37963634" target="_blank">37963634</a><a href="/pmc/articles/PMC10644209" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35531751">Do we need audiogram-based prescriptions? A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Almufarrij I,
Dillon H,
Munro KJ</span><br />
<span class="medgenPMjournal">Int J Audiol</span>
2023 Jun;62(6):500-511.
Epub 2022 May 9
doi: 10.1080/14992027.2022.2064925.
<span class="bold">PMID: </span><a href="/pubmed/35531751" target="_blank">35531751</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34233329">Betahistine in Ménière's Disease or Syndrome: A Systematic Review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Van Esch B,
van der Zaag-Loonen H,
Bruintjes T,
van Benthem PP</span><br />
<span class="medgenPMjournal">Audiol Neurootol</span>
2022;27(1):1-33.
Epub 2021 Jul 7
doi: 10.1159/000515821.
<span class="bold">PMID: </span><a href="/pubmed/34233329" target="_blank">34233329</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33151295">Cochlear Implantation in Children With Single-Sided Deafness: A Systematic Review and Meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Benchetrit L,
Ronner EA,
Anne S,
Cohen MS</span><br />
<span class="medgenPMjournal">JAMA Otolaryngol Head Neck Surg</span>
2021 Jan 1;147(1):58-69.
doi: 10.1001/jamaoto.2020.3852.
<span class="bold">PMID: </span><a href="/pubmed/33151295" target="_blank">33151295</a><a href="/pmc/articles/PMC7645748" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32192585">Drug-associated adverse events in the treatment of multidrug-resistant tuberculosis: an individual patient data meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lan Z,
Ahmad N,
Baghaei P,
Barkane L,
Benedetti A,
Brode SK,
Brust JCM,
Campbell JR,
Chang VWL,
Falzon D,
Guglielmetti L,
Isaakidis P,
Kempker RR,
Kipiani M,
Kuksa L,
Lange C,
Laniado-Laborín R,
Nahid P,
Rodrigues D,
Singla R,
Udwadia ZF,
Menzies D;
Collaborative Group for the Meta-Analysis of Individual Patient Data in MDR-TB treatment 2017</span><br />
<span class="medgenPMjournal">Lancet Respir Med</span>
2020 Apr;8(4):383-394.
Epub 2020 Mar 17
doi: 10.1016/S2213-2600(20)30047-3.
<span class="bold">PMID: </span><a href="/pubmed/32192585" target="_blank">32192585</a><a href="/pmc/articles/PMC7384398" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Deafness%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 (360)</a></div></div>
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0011053%5bDISCUI%5d&amp;filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (4)</a></li>
<li><a href="/gtr/tests?term=C0011053%5bDISCUI%5d&amp;filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (6)</a></li>
<li><a href="/gtr/tests?term=C0011053%5bDISCUI%5d&amp;filter=method%3A2%5F19" target="_blank">Targeted variant analysis (1)</a></li>
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0011053%5bDISCUI%5d" target="_blank">See all (7)</a></total></li>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Deafness" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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