Phenotype #0000355107
| Individual ID |
00469962 |
| Associated disease |
? |
| Diagnosis/Initial |
Joubert syndrome |
| Diagnosis/Definite |
- |
| Phenotype details |
infantile hypotonia; normal breathing; 8m-sit; 14m-walk; speech delay; persistent congenital ocular-motor apraxia; no ataxia; frontal bossing; no intellectual disability; MRI brain superior cerebellar peduncles; superior cerebellar dysplasia; vermis hypoplasia; Vermian split; fastigium displaced |
| Inheritance |
Familial |
| Age/Examination |
05y-10y |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Valentina Serpieri |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-08-22 15:57:28 +02:00 (CEST) |
| Date last edited |
N/A |
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