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Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome

Disease definition

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.


Classification level: Disorder
  • Synonym(s):
    • Poretti-Boltshauser syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: G11.1
  • OMIM: 615960
  • UMLS: C4014821
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

Disease review articles


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