Spastic paraplegia 6, autosomal dominant: A rare genetic disorder characterized by progressive leg spasticity and weakness. More detailed information about the symptoms, causes, and treatments of Spastic paraplegia 6, autosomal dominant is available below.
See full list of 10 symptoms of Spastic paraplegia 6, autosomal dominant
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Spastic paraplegia 6, autosomal dominant is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Spastic paraplegia 6, autosomal dominant, or a subtype of Spastic paraplegia 6, autosomal dominant,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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