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Article

Clinical Details of Low-Frequency Hearing Loss Observed in Autosomal Dominant MYO7A-Associated Hearing Loss Patients.

Genes - 11 Mar 2026

Koizumi Hiromi, Nishio Shin-Ya, Usami Shin-Ichi

Abstract excerpt

BACKGROUND/OBJECTIVES: MYO7A is known to be the genetic cause of Usher syndrome type 1, as well as autosomal dominant and autosomal recessive non-syndromic hearing loss. In general, autosomal dominant MYO7A-associated hearing loss shows progressive high-frequency, sloping hearing loss. However, several variants are associated with low-frequency hearing loss. MYO7A-associated low-frequency hearing loss is...

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Identifiers

PMID: 41898848
DOI: 10.3390/genes17030314
PMCID: PMC13026303

Genes

MYO7A

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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