About The Medical Condition Autosomal Dominant Striatonigral Degeneration
Find the definition of the medical term Autosomal Dominant Striatonigral Degeneration. Autosomal Dominant Striatonigral Degeneration defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Autosomal Dominant Striatonigral Degeneration
Autosomal Dominant Striatonigral Degeneration Medical Condition |
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What's The Definition Of The Medical Condition Autosomal Dominant Striatonigral Degeneration?
A dominantly-inherited ataxia first described in people of Azorean and Portuguese descent, and subsequently identified in Brazil, Japan, China, and Australia. This disorder is classified as one of the SPINOCEREBELLAR ATAXIAS (Type 3) and has been associated with a mutation of the MJD1 gene on chromosome 14. Clinical features include progressive ataxia, dysarthria, postural instability, nystagmus, eyelid retraction, and facial fasciculations. Dystonia is prominent in younger patients (referred to as Type I Machado-Joseph Disease). Type II features ataxia and ocular signs; Type III features muscle atrophy and a sensorimotor neuropathy; and Type IV features extrapyramidal signs combined with a sensorimotor neuropathy. (From Clin Neurosci 1995;3(1):17-22; Ann Neurol 1998 Mar;43(3):288-96)
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