Conditions / Genetic
dystonia 30
info ยท Genetic
A dystonia characterized by the onset of symptoms in the first decades of life, with oromandibular, cervical, bulbar, or upper limb dystonia, and usually show slow progression to generalized dystonia. Some patients may lose ambulation and have neurocognitive i
A dystonia characterized by the onset of symptoms in the first decades of life, with oromandibular, cervical, bulbar, or upper limb dystonia, and usually show slow progression to generalized dystonia. Some patients may lose ambulation and have neurocognitive impairment, including mild intellectual disability or psychiatric manifestations with has_material_basis_in heterozygous mutation in the VPS16 gene on chromosome 20p13.
Signs and symptoms
- Dystonia
- Torticollis
- Globus pallidus hypointensity on susceptibility-weighted imaging
- Diffuse cerebral atrophy
- Writer's cramp
- Moderate intellectual disability
- Leg dystonia
- Arm dystonia
- Oromandibular dystonia
- Loss of ambulation
Also known as: DYT30