Familial syndrome of deafness, myoclonus, and cerebellar ataxia.
作者信息
Chayasirisobhon S, Walters B
出版信息
Neurology. 1984 Jan;34(1):78-9. doi: 10.1212/wnl.34.1.78.
PMID:6537856
Abstract
We report a case of identical twins with progressive sensorineural hearing loss, myoclonus, intention tremor, and ataxia. The involved member of the family may suggest of autosomal dominant transmission with variable penetrance.
摘要
Zotero 插件