SPG8 (medical condition): A rare form of muscle spasticity and weakness that affects mainly the lower legs.
See also:
Spastic paraplegia 8, autosomal dominant:
»Introduction: Spastic paraplegia 8, autosomal dominant
»Symptoms of Spastic paraplegia 8, autosomal dominant
SPG8 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SPG8, or a subtype of SPG8,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
SPG8: Another name for Spastic paraplegia 8, autosomal dominant (or close medical condition association).
»Introduction: Spastic paraplegia 8, autosomal dominant
»Symptoms of Spastic paraplegia 8, autosomal dominant
Some of the symptoms of SPG8 incude:
Read more about symptoms of SPG8 (Spastic paraplegia 8, autosomal dominant)
Source - NIH
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