Huntington disease-like 3

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

12 clinical trials for this condition and its sub-types, 0 tagged with Huntington disease-like 3 itself.