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Article

Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder.

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery - 1 Nov 2016

Wasano Koichiro, Matsunaga Tatsuo, Ogawa Kaoru, Kunishima Shinji

Abstract excerpt

MYH9 disorder is a rare autosomal-dominant disorder. We previously reported that it is caused by mutations in the gene for nonmuscle myosin heavy chain IIA (NMMHC-IIA). MYH9 disorder causes congenital macrothrombocytopenia accompanied by progressive sensorineural hearing loss, nephropathy, and cataract. However, there are few reports that describe the audiological features of MYH9 disorder. The objective of this...

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Source

Identifiers

PMID: 26942920
DOI: 10.1007/s00405-016-3954-0

Genes

MYH9

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder.PMID 26942920Read ↗

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