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Article

Genetic etiology of hearing loss in Iran.

Human genetics - 1 Apr 2022

Babanejad Mojgan, Beheshtian Maryam, Jamshidi Fereshteh, Mohseni Marzieh, Booth Kevin T, Kahrizi Kimia, Najmabadi Hossein

Abstract excerpt

Hearing loss (HL) is an etiologically heterogeneous disorder that affects around 5% of the world's population. There has been an exponential increase in the identification of genes and variants responsible for hereditary HL over recent years. Iran, a country located in the Middle East, has a high prevalence of consanguineous marriages, so heterogeneous diseases such as HL are more common. Comprehensive studies...

Read the complete abstract on PubMed

Topics

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Share to Deafness
Share to Ear Surgery and Otitis Media
Share to Hearing, Cochlea, Tinnitus, Genetics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Hearing Loss, Sensorineural

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Source

Identifiers

PMID: 35050400
DOI: 10.1007/s00439-021-02421-w

Genes

CDH23
GJB2
MYO15A
MYO7A
SLC26A4
TMC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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