Progressive cerebello-cerebral atrophy

Orpha code: 247198OMIM code: 615851

Definicja

A rare genetic neurological disorder characterized by postnatal onset of severe global developmental delay, profound mental retardation, progressive microcephaly, progressive spasticity evolving into spastic quadriplegia with joint contractures, generalized seizures, and irritability. Severe choreoathetosis and dysmorphic features are absent. Brain imaging shows progressive cerebellar atrophy followed by cerebral atrophy affecting both white and grey matter, but no pontine involvement.

Disease data
Klasyfikacja

Disease

Synonimy
PCCA
PCCA
Kod ORPHA
247198
Kod OMIM
615851
Kod ICD10
G31.8
Kod ICD11
-

No additional description.

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