作者: Henry Paulson , Puneet Opal
DOI: 10.1007/978-1-59259-006-3_12
关键词: Spinocerebellar ataxia 、 Disease 、 Ataxia 、 Pathophysiology 、 Neuroscience 、 Confusion 、 Medicine
摘要: Once thought to be rare, spinocerebellar ataxia type 3 (SCA3) is now believed the most common dominantly inherited ataxia. Of polyglutamine disorders described date, SCA3 has perhaps interesting history—one that reflects past confusion about clinical spectrum of this remarkably pleiotropic disease.