Literature DB >> 32243624

Genetics of Postlingual Sensorineural Hearing Loss.

Shadi Ahmadmehrabi1,2, Jason Brant3, Douglas J Epstein2, Michael J Ruckenstein3, Daniel J Rader2.   

Abstract

Literature and clinical practice around adult-onset hearing loss (HL) has traditionally focused on environmental risk factors, including noise exposure, ototoxic drug exposure, and cardiovascular disease. The most common diagnosis in adult-onset HL is presbycusis. However, the age of onset of presbycusis varies, and patients often describe family history of HL as well as individual variation in progression and severity. In recent years, there has been accumulating evidence of gene-environment interactions underlying adult cases of HL. Susceptibility loci for age-related HL have been identified, and genes related to postlingual nonsyndromic HL continue to be discovered through individual reports and genome-wide association studies. This review will outline main concepts in genetics as related to HL, identify implicated genes, and discuss clinical implications. Laryngoscope, 131:401-409, 2021.
© 2020 The American Laryngological, Rhinological and Otological Society, Inc.

Entities:  

Keywords:  Genetics; hearing loss; sensorineural hearing loss

Mesh:

Year:  2020        PMID: 32243624     DOI: 10.1002/lary.28646

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  5 in total

1.  Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults.

Authors:  Shadi Ahmadmehrabi; Binglan Li; Joseph Park; Batsal Devkota; Marijana Vujkovic; Yi-An Ko; David Van Wagoner; W H Wilson Tang; Ian Krantz; Marylyn Ritchie; Jason Brant; Michael J Ruckenstein; Douglas J Epstein; Daniel J Rader
Journal:  Hum Genet       Date:  2021-03-21       Impact factor: 4.132

2.  Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss.

Authors:  Dominika Oziębło; Sang-Yeon Lee; Marcin Ludwik Leja; Byung Yoon Choi; Monika Ołdak; Anna Sarosiak; Natalia Bałdyga; Henryk Skarżyński; Yehree Kim; Jin Hee Han; Hyo Soon Yoo; Min Hyun Park
Journal:  Hum Genet       Date:  2022-03-07       Impact factor: 4.132

3.  Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss.

Authors:  Roxane Van Heurck; Maria Teresa Carminho-Rodrigues; Emmanuelle Ranza; Caterina Stafuzza; Lina Quteineh; Corinne Gehrig; Eva Hammar; Michel Guipponi; Marc Abramowicz; Pascal Senn; Nils Guinand; Helene Cao-Van; Ariane Paoloni-Giacobino
Journal:  Genes (Basel)       Date:  2021-08-20       Impact factor: 4.096

4.  Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains.

Authors:  Sun Young Joo; Gina Na; Jung Ah Kim; Jee Eun Yoo; Da Hye Kim; Se Jin Kim; Seung Hyun Jang; Seyoung Yu; Hye-Youn Kim; Jae Young Choi; Heon Yung Gee; Jinsei Jung
Journal:  Biomedicines       Date:  2022-03-29

5.  Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation.

Authors:  Chang Guo; Sha-Sha Huang; Yong-Yi Yuan; Ying Zhou; Ning Wang; Dong-Yang Kang; Su-Yan Yang; Xin Zhang; Xue Gao; Pu Dai
Journal:  Neural Plast       Date:  2020-08-01       Impact factor: 3.599

  5 in total

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