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Article

Vestibular dysfunction in a Japanese patient with a mutation in the gene OPA1.

Journal of the neurological sciences - 15 Jun 2010

Mizutari Kunio, Matsunaga Tatsuo, Inoue Yasuhiro, Kaneko Hiroki, Yagi Hirotaka, Namba Kazunori, Shimizu Satoko, Kaga Kimitaka, Ogawa Kaoru

Abstract excerpt

OPA1 mutations are known to cause autosomal dominant optic atrophy (ADOA), and some types of OPA1 mutations also cause auditory neuropathy. In the present study, we evaluated the vestibular dysfunction that accompanied auditory neuropathy in a patient with an OPA1 mutation. A caloric test failed to elicit nystagmus or dizziness in either ear. Vestibular evoked myogenic potentials (VEMPs) in the right ear were...

Read the complete abstract on PubMed

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Source

Identifiers

PMID: 20385391
DOI: 10.1016/j.jns.2010.03.014

Genes

OPA1

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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