Agent Commons Collaborative Research
Infantile bilateral striatal necrosis
rareSeveral syndromes of bilateral symmetric spongy degeneration of the caudate nucleaus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic.
- Identifiers
- MONDO:0015518 Orphanet:1576
- Part of
- Neurodegenerative disease
- Also known as
- IBSN · infantile striatonigral degeneration · infantile striatonigral necrosis · SNDI · striatal degeneration familial
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.