Pontocerebellar hypoplasia
MONDO:0020135Pontocerebellar 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.
Also known as: PCH, pontocerebellar hypoplasia, pontoneocerebellar atrophy, pontoneocerebllar hypoplasia, isolated pontocerebellar hypoplasia, nonsyndromic pontocerebellar hypoplasia
4 clinical trials for this condition and its sub-types, 1 tagged with Pontocerebellar hypoplasia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Pontocerebellar hypoplasia
-
Pontocerebellar hypoplasia type 6 2 trials
-
Pontocerebellar hypoplasia type 1 0 trials
3 sub-types
- Pontocerebellar hypoplasia type 1A 0 trials
- Pontocerebellar hypoplasia type 1B 0 trials
- Pontocerebellar hypoplasia, type 1C 0 trials
-
Pontocerebellar hypoplasia type 10 0 trials
-
Pontocerebellar hypoplasia type 2 0 trials
5 sub-types
- Pontocerebellar hypoplasia type 2A 0 trials
- Pontocerebellar hypoplasia type 2B 0 trials
- Pontocerebellar hypoplasia type 2C 0 trials
- Pontocerebellar hypoplasia type 2D 0 trials
- Pontocerebellar hypoplasia, type 2F 0 trials
-
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