Agent Commons Collaborative Research

Early-onset parkinsonism-intellectual disability syndrome

rare

A 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.

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

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