Anemia, sideroblastic spinocerebellar ataxia: A rare inherited condition characterized by anemia at birth as well as spinocerebellar ataxia (impaired ability to control voluntary movements). More detailed information about the symptoms, causes, and treatments of Anemia, sideroblastic spinocerebellar ataxia is available below.
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Anemia, sideroblastic spinocerebellar ataxia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Anemia, sideroblastic spinocerebellar ataxia, or a subtype of Anemia, sideroblastic spinocerebellar ataxia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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