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See Latest ArticlesVestibular Impairment in a Dutch DFNA15 Family with an L289F Mutation in POU4F3
Audiology & Neuro-Otology, 04/23/09
Drunen FJWB et al. - Vestibular involvement appeared to be present in 2 affected individuals according to their medical history. Vestibular examination results in an extended subset of L289F POU4F3 mutation carriers varied from normal to areflexia. DFNA15 is the third cochleovestibular disorder, after DFNA9 and DFNA11, in the autosomal dominant nonsyndromic hearing impairment.
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