Huntington disease-like 3

MONDO:0011487

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.

Also known as: HDL3, Huntington disease-like 3, Huntington disease-like type 3, Huntington disease-like neurodegenerative disorder, autosomal recessive

166 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by