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Striatonigral degeneration

rare

A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements.

Identifiers
MONDO:0003122
Part of
Inborn errors of metabolismInherited neurodegenerative disorderMultiple system atrophy

Subtypes

All diseases Rare only
Disease Subtypes
Striatal degeneration, autosomal dominant 2
Familial infantile bilateral striatal necrosis 1
Striatonigral degeneration, childhood-onset

Rare disease

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