| Individual ID |
00151926 |
| Associated disease |
WHS |
| Phenotype details |
2y1m-onset seizures; no status epilepticus; severe developmental delay, 7y-walking; height/weight (SD) -4.9/-3.0; oral feeding; no cleft lip/cleft palate; no heart defect; no urogenital defect; Strabismus (esotropia); no hearing impairment; |
| Diagnosis/Initial |
Wolf-Hirschhorn syndrome |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
WHS |
| Age/Examination |
16y (16 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-01-28 09:38:22 +01:00 (CET) |
| Date last edited |
2018-01-28 10:21:36 +01:00 (CET) |