## Abstract Spinocerebellar ataxias are heterogeneous disorders with overlapping clinical features. Spinocerebellar ataxiaβ6 is a dominantly inherited condition characterized by relatively pure ataxia with a paucity of other manifestations including extrapyramidal findings. We report on two patient
β¦ LIBER β¦
Morphological Purkinje cell changes in spinocerebellar ataxia type 6
β Scribed by Q. Yang; Y. Hashizume; M. Yoshida; Y. Wang; Y. Goto; N. Mitsuma; K. Ishikawa; H. Mizusawa
- Publisher
- Springer-Verlag
- Year
- 2000
- Tongue
- English
- Weight
- 342 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0001-6322
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## Abstract We report on a family with ataxia type 6 (SCA6) showing peculiar oculomotor symptoms. The proband presented with periodic alternating nystagmus (PAN), and her 2 brothers had rebound nystagmus and gazeβevoked nystagmus. They carried the identical mutation (the number of expanded CAG repe