Spastic paraplegia 11, autosomal recessive: A rare genetic disorder characterized by progressive spasticity and weakness of the lower legs as well as mental retardation. More detailed information about the symptoms, causes, and treatments of Spastic paraplegia 11, autosomal recessive is available below.
See full list of 10 symptoms of Spastic paraplegia 11, autosomal recessive
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Prognosis for Spastic paraplegia 11, autosomal recessive: wheelchair use usually during 2nd decade
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Spastic paraplegia 11, autosomal recessive 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 11, autosomal recessive, or a subtype of Spastic paraplegia 11, autosomal recessive,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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