Pathophysiology of SCA3

作者: Henry Paulson , Puneet Opal

DOI: 10.1007/978-1-59259-006-3_12

关键词: Spinocerebellar ataxiaDiseaseAtaxiaPathophysiologyNeuroscienceConfusionMedicine

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.

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