neurodegenerative disorder with cerebellar and caudate atrophy

Huntington 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.

Therapeutic area

Neurology

Rarity

Unknown

Prevalence

—

MONDO

MONDO:0981024