## Abstract Dominantly inherited ataxias resulting from different gene mutations are difficult to distinguish based on clinical phenotypes. We believe the phenotypic variability within families can be a clue to clinical diagnosis. We illustrate the range of phenotypes extending from levodopa‐respon
Eyelid dystonia in Machado-Joseph Disease
✍ Scribed by Francisco Cardoso; José Teotonio de Oliveira; Marzia Puccioni-Sohler; Alexandre R. Fernandes; James Pitágoras de Mattos; Iscia Lopes-Cendes
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 475 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0885-3185
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## Abstract Machado‐Joseph disease (MJD) is an autosomal dominant spinocerebellar ataxia. Few studies have examined the neuropsychological and neurobehavioral profiles of patients with MJD. In this study, six individuals with MJD were given a battery of neuropsychological tests. Relative impairment
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