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Up to: Hereditary neurological disease · Central nervous system malformation

Pontocerebellar hypoplasia

Pontocerebellar hypoplasias (PCH) are a rare heterogeneous group of diseases characterized by hypoplasia and atrophy and/or early neurodegeneration of the cerebellum and pons. Eight subtypes named type 1-8 have been described, generally inherited in an autosomal recessive pattern.

1 trial tagged with this condition →

Pontocerebellar hypoplasia type 6 2 trials
Pontocerebellar hypoplasia type 1 0 trials Sub-types →
Pontocerebellar hypoplasia type 10 0 trials
Pontocerebellar hypoplasia type 2 0 trials Sub-types →
Pontocerebellar hypoplasia type 2E 0 trials
Pontocerebellar hypoplasia type 3 0 trials
Pontocerebellar hypoplasia type 4 0 trials
Pontocerebellar hypoplasia type 5 0 trials
Pontocerebellar hypoplasia type 7 0 trials
Pontocerebellar hypoplasia type 8 0 trials
Pontocerebellar hypoplasia type 9 0 trials
Pontocerebellar hypoplasia, IIA 17 0 trials
Pontocerebellar hypoplasia, type 11 0 trials
Pontocerebellar hypoplasia, type 12 0 trials
Pontocerebellar hypoplasia, type 13 0 trials
Pontocerebellar hypoplasia, type 14 0 trials
Pontocerebellar hypoplasia, type 15 0 trials
Pontocerebellar hypoplasia, type 16 0 trials
Pontocerebellar hypoplasia, type 1D 0 trials
Pontocerebellar hypoplasia, type 1E 0 trials
Pontocerebellar hypoplasia, type 1F 0 trials