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Non-syndromic pontocerebellar hypoplasia

ORPHA:98523

Definition

A rare group of neurodegenerative disorders with a prenatal onset characterized by hypoplasia and/or atrophy of the cerebellum and pons. Involvement of supratentorial structures is variable. Multiple forms have been described based on severity, age of onset and clinical presentation.

Prevalence
Unknown
Inheritance
Autosomal recessive
Age of onset
Antenatal, Infancy, Neonatal