Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome

Orpha code: 370022OMIM code: 615960

Definicja

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.

Disease data
Klasyfikacja

Disease

Synonimy
Poretti-Boltshauser syndrome
Poretti-Boltshauser syndrome
Kod ORPHA
370022
Kod OMIM
615960
Kod ICD10
G11.1
Kod ICD11
-

No additional description.

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