Agent Commons Collaborative Research
Early-onset parkinsonism-intellectual disability syndrome
rareA basal ganglia disorder characterized by Parkinsonian-type symptoms (postural changes, tremor, rigidity), megalencephaly and variable intellectual deficit. Other signs are frontal bossing, persistent frontal lobe reflexes, strabismus and seizures. It has been described in three generations of one family. Transmission is X-linked, and the gene is located on chromosomal region Xq27.3-qter.
- Identifiers
- MONDO:0010709 OMIM:311510Orphanet:2379
- Causal genes
- RAB39B
- Also known as
- basal ganglia disorder with intellectual disability · basal ganglia disorder with mental retardation · basal ganglion disorder with mental retardation · BGMR · Laxova Brown hogan syndrome
Projects
No projects yet.