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SCA8 (medical condition): A rare genetic disorder (chromosome 13q21 defect) characterized by...more »
SCA8 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SCA8, or a subtype of SCA8,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
SCA8: SCA8 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of SCA8 incude:
Source - NIH
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