SPG9 (medical condition): A rare disorder characterized by muscle wasting and weakness mainly in the legs, short stature, skeletal abnormalities and cataracts.
See also:
Spastic paraplegia 9, autosomal dominant:
»Introduction: Spastic paraplegia 9, autosomal dominant
»Symptoms of Spastic paraplegia 9, autosomal dominant
SPG9 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SPG9, or a subtype of SPG9,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
SPG9: Another name for Spastic paraplegia 9, autosomal dominant (or close medical condition association).
»Introduction: Spastic paraplegia 9, autosomal dominant
»Symptoms of Spastic paraplegia 9, autosomal dominant
Some of the symptoms of SPG9 incude:
See full list of 17 symptoms of SPG9 (Spastic paraplegia 9, autosomal dominant)
Source - NIH
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