Striatonigral degeneration infantile (medical condition): A genetic neurological disorder caused by progressive damage to a part of the brain called the striatum.
See also:
Striatonigral degeneration infantile:
»Introduction: Striatonigral degeneration infantile
»Symptoms of Striatonigral degeneration infantile
These medical condition or symptom topics may be relevant to medical information for Striatonigral degeneration infantile:
Striatonigral degeneration infantile is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Striatonigral degeneration infantile, or a subtype of Striatonigral degeneration infantile,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Striatonigral degeneration infantile as a "rare disease".
Source - Orphanet
Striatonigral degeneration infantile (medical condition): See Striatonigral degeneration infantile (disease information).
»Introduction: Striatonigral degeneration infantile
»Symptoms of Striatonigral degeneration infantile
Source - NIH
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