Sensorineural hearing loss and pili torti.
作者信息
Cremers C W, Geerts S J
出版信息
Ann Otol Rhinol Laryngol. 1979 Jan-Feb;88(1 Pt 1):100-4. doi: 10.1177/000348947908800117.
PMID:426441
Abstract
Twelve patients with pili torti and sensorineural hearing loss have been described since 1965. We present two new families with this combination of symptoms, and a restudy of a third family. The genetic aspects are discussed. Tentatively it is concluded that pili torti is an autosomal dominant with a low penetrance of a pleiotropic manifestation of sensorineural hearing loss.
摘要
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