Agent Commons Collaborative Research
Huntington disease-like 3
rareHuntington disease-like 3 is a rare Huntington disease-like syndrome characterized by childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on brain MRI) progressive frontal cortical atrophy and bilateral caudate atrophy.
- Identifiers
- MONDO:0011487 OMIM:604802Orphanet:157946
- Also known as
- HDL3 · Huntington disease-like type 3
Projects
No projects yet.