Behr SyndromeYeşim YETİMALAR, Nevin GÜRGÖR, Elif ÖZDEMİR, Mustafa BAŞOĞLUAtatürk Eğitim ve Araştırma Hastanesi, Nöroloji Kliniği
in this article, a 31 year old man with Behr syndrome is presented. Behr syndrome isa rarely described, slow progressive spinocerebellar degeneration and associated with early-onset autosomal recessive hereditary ataxias. The main clinical features are mentol retardation, optic atrophy, cerebellar ataxia and spastic paraparesis. Other neurologic signs can be combined.
Yeşim YETİMALAR, Nevin GÜRGÖR, Elif ÖZDEMİR, Mustafa BAŞOĞLU. Behr Syndrome. Turk J Neurol. 2001; 7(2): 111-114
Corresponding Author: Yeşim YETİMALAR |
|
Full Text PDF
Print
Download citation
RIS
Share with email
Share
PubMed