Progressive cerebello-cerebral atrophy

Orpha code: 247198OMIM code: 615851

Definition

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
Classification

Disease

Synonyms
PCCA
PCCA
ORPHA code
247198
OMIM code
615851
ICD10 code
G31.8
ICD11 code
-

No additional description.

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