| Literature DB >> 34599368 |
Ana Carla Batissoco1,2, Vinicius Pedroso-Campos1, Eliete Pardono1,3, Juliana Sampaio-Silva1, Cindy Yukimi Sonoda1, Gleiciele Alice Vieira-Silva1, Estefany Uchoa da Silva de Oliveira Longati1, Diego Mariano4, Ana Cristina Hiromi Hoshino2, Robinson Koji Tsuji2, Rafaela Jesus-Santos1, Osório Abath-Neto5, Ricardo Ferreira Bento1,2, Jeanne Oiticica1,2, Karina Lezirovitz6,7.
Abstract
Hearing loss is one of the most common sensory defects, affecting 5.5% of the worldwide population and significantly impacting health and social life. It is mainly attributed to genetic causes, but their relative contribution reflects the geographical region's socio-economic development. Extreme genetic heterogeneity with hundreds of deafness genes involved poses challenges for molecular diagnosis. Here we report the investigation of 542 hearing-impaired subjects from all Brazilian regions to search for genetic causes. Biallelic GJB2/GJB6 causative variants were identified in 12.9% (the lowest frequency was found in the Northern region, 7.7%), 0.4% carried GJB2 dominant variants, and 0.6% had the m.1555A > G variant (one aminoglycoside-related). In addition, other genetic screenings, employed in selected probands according to clinical presentation and presumptive inheritance patterns, identified causative variants in 2.4%. Ear malformations and auditory neuropathy were diagnosed in 10.8% and 3.5% of probands, respectively. In 3.8% of prelingual/perilingual cases, Waardenburg syndrome was clinically diagnosed, and in 71.4%, these diagnoses were confirmed with pathogenic variants revealed; seven out of them were novel, including one CNV. All these genetic screening strategies revealed causative variants in 16.2% of the cases. Based on causative variants in the molecular diagnosis and genealogy analyses, a probable genetic etiology was found in ~ 50% of the cases. The present study highlights the relevance of GJB2/GJB6 as a cause of hearing loss in all Brazilian regions and the importance of screening unselected samples for estimating frequencies. Moreover, when a comprehensive screening is not available, molecular diagnosis can be enhanced by selecting probands for specific screenings.Entities:
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Year: 2021 PMID: 34599368 DOI: 10.1007/s00439-021-02372-2
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132