Striatonigral degeneration

MONDO:0003122

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.

12 clinical trials for this condition and its sub-types, 0 tagged with Striatonigral degeneration itself.

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↑ Inborn errors of metabolism (2228) ↑ Inherited neurodegenerative disorder (807) ↑ Multiple system atrophy (119)

Sub-types of Striatonigral degeneration

Familial infantile bilateral striatal necrosis 0 trials
1 sub-type
- Striatonigral degeneration, infantile, mitochondrial 0 trials
Striatal degeneration, autosomal dominant 0 trials
2 sub-types
- Autosomal dominant striatal neurodegeneration type 1 0 trials
- Striatal degeneration, autosomal dominant 2 0 trials
Striatonigral degeneration, childhood-onset 0 trials

Including sub-types (12) Tagged with Striatonigral degeneration (0)

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