Conditions / Genetic
Parkinson's disease 19A
info · Genetic · ICD-10: G20
An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.
Signs and symptoms
- Bradykinesia
- Dysarthria
- Pill-rolling tremor
- Postural instability
- Glabellar reflex
- Limb hypertonia
- Hypomimic face
- Loss of ambulation
- Hypometric saccades
- Parkinsonism
Also known as: juvenile onset Parkinson disease 19A; juvenile onset Parkinson's disease 19A