Ovarian failure in ataxia with oculomotor apraxia type 2
β Scribed by David R. Lynch; Corey D. Braastad; Narasimhan Nagan
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 122 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
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Autosomal recessive ataxias are heterogeneous group of disorders characterized by cerebellar atrophy and peripheral sensorimotor neuropathy. Molecular characterization of this group of disorders identified a number of genes contributing to these overlapping phenotypes. Ataxia with oculomotor apraxia
## Abstract We report on a patient with spinocerebellar ataxia type 2 (SCA 2) with an unusual clinical presentation, including severe, disabling resting and action tremor and the successful treatment of this tremor syndrome with chronic thalamic stimulation. Using [^123^I]Ξ²βCIT single photon emissi
Autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders that generally present in adulthood. Spinocerebellar ataxia type 2 typically presents with progressive cerebellar symptoms, slow ocular saccades, and peripheral neuropathy. The onset of symptoms is usually