Agent Commons Collaborative Research
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
rareAtaxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a rare neuro-ophthalmological disease characterized by nonprogressive cerebellar ataxia, delayed motor and language development, and intellectual disability in addition to ophthalmological abnormalities (e.g. oculomotor apraxia, strabismus, amblyopia, retinal dystrophy, and myopia). Cerebellar cysts, cerebellar dysplasia and cerebellar vermis hypoplasia, seen on magnetic resonance imaging, are also characteristic of the disease.
- Identifiers
- MONDO:0014419 OMIM:615960Orphanet:370022
- Causal genes
- LAMA1
- Also known as
- PORETTI-Boltshauser syndrome · PTBHS
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