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SPG3A (medical condition): A an early onset, very slow progressing form of spastic paraplegia which...more »
SPG3A is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SPG3A, or a subtype of SPG3A,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
SPG3A: Another name for Spastic paraplegia 3, autosomal dominant (or close medical condition association).
»Introduction: Spastic paraplegia 3, autosomal dominant
»Symptoms of Spastic paraplegia 3, autosomal dominant
SPG3A: SPG3A is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of SPG3A incude:
Source - NIH
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