Spastic paraplegia 19, autosomal dominant: A rare genetic disorder characterized mainly by progressive spasticity and weakness of the lower legs. The condition is generally slow progressing with wheelchair confinement occurring only rarely. More detailed information about the symptoms, causes, and treatments of Spastic paraplegia 19, autosomal dominant is available below.
See full list of 7 symptoms of Spastic paraplegia 19, autosomal dominant
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Spastic paraplegia 19, 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 19, autosomal dominant, or a subtype of Spastic paraplegia 19, autosomal dominant,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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