| Literature DB >> 33111345 |
Zippora Brownstein1, Suleyman Gulsuner2, Tom Walsh2, Fábio T A Martins1, Shahar Taiber1, Ofer Isakov3, Ming K Lee2, Mor Bordeynik-Cohen1, Maria Birkan1,4, Weise Chang5, Silvia Casadei2, Nada Danial-Farran1,6,7, Amal Abu-Rayyan1,8, Ryan Carlson2, Lara Kamal8, Asgeir Ö Arnthórsson9, Meirav Sokolov1,10, Dror Gilony1,10, Noga Lipschitz1,11, Moshe Frydman1,12, Bella Davidov4, Michal Macarov13, Michal Sagi13, Chana Vinkler14, Hana Poran12, Reuven Sharony15, Nadra Samra16, Na'ama Zvi13, Hagit Baris-Feldman17, Amihood Singer18, Ophir Handzel19, Ronna Hertzano20, Doaa Ali-Naffaa1,21, Noa Ruhrman-Shahar4, Ory Madgar11, Efrat Sofrin-Drucker4, Amir Peleg21, Morad Khayat6, Mordechai Shohat1,22,23, Lina Basel-Salmon1,4, Elon Pras1,12, Dorit Lev1,14, Michael Wolf11, Eirikur Steingrimsson9, Noam Shomron3, Matthew W Kelley5, Moien N Kanaan8, Stavit Allon-Shalev6,7, Mary-Claire King2, Karen B Avraham1.
Abstract
Mutations in more than 150 genes are responsible for inherited hearing loss, with thousands of different, severe causal alleles that vary among populations. The Israeli Jewish population includes communities of diverse geographic origins, revealing a wide range of deafness-associated variants and enabling clinical characterization of the associated phenotypes. Our goal was to identify the genetic causes of inherited hearing loss in this population, and to determine relationships among genotype, phenotype, and ethnicity. Genomic DNA samples from informative relatives of 88 multiplex families, all of self-identified Jewish ancestry, with either non-syndromic or syndromic hearing loss, were sequenced for known and candidate deafness genes using the HEar-Seq gene panel. The genetic causes of hearing loss were identified for 60% of the families. One gene was encountered for the first time in human hearing loss: ATOH1 (Atonal), a basic helix-loop-helix transcription factor responsible for autosomal dominant progressive hearing loss in a five-generation family. Our results show that genomic sequencing with a gene panel dedicated to hearing loss is effective for genetic diagnoses in a diverse population. Comprehensive sequencing enables well-informed genetic counseling and clinical management by medical geneticists, otolaryngologists, audiologists, and speech therapists and can be integrated into newborn screening for deafness.Entities:
Keywords: deafness; diagnostics; gene panel; genomics; hearing; massively parallel sequencing; next‐generation sequencing
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Year: 2020 PMID: 33111345 PMCID: PMC8045518 DOI: 10.1111/cge.13817
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.296