| Individual ID |
00207424 |
| Associated disease |
GA1 |
| Inheritance |
Familial, autosomal recessive |
| Age/Onset |
00y05m |
| Diagnosis/Initial |
- |
| Age/Examination |
- |
| Diagnosis/Definite |
- |
| Age/Diagnosis |
00y07m |
| Phenotype/Onset |
- |
| Phenotype details |
Severely affected (bedridden, tube feeding required); Symptoms: seizure (HP:0001250), regression (HP:0002376), hypertonia (HP:0001276); Precipitating factor: infection; Neuroimaging: frontotemporal atrophy, striatum signal abnormalities |
| Protein |
- |
| Biochem |
GA(urine): high, glutarylcarnitine(dried blood spot): not determined |
| Enzyme/Activity |
≤ 5% (lymphoblasts and cultured fibroblasts) |
| Owner name |
Isabelle Rinke |
| Database submission license |
No license selected |
| Created by |
Isabelle Rinke |
| Date created |
2018-11-22 09:29:02 +01:00 (CET) |
| Date last edited |
2018-11-22 15:23:45 +01:00 (CET) |