Phenotype #0000307835
| Individual ID |
00416069 |
| Associated disease |
COQ10D |
| Phenotype details |
see paper; ... (esp. treatment), microcephaly; birth full term; dystrophy, microcephaly; delayed motor development; delayed cognitive development; developmental stagnation/minimal development; infancy spasticity; tetraparesis/paraparesis; truncal hypotonia; 8w-seizures, focal, secondarily generalized; no stroke like episodes; encephalopathy; no respiratory distress/insufficiency; feeding difficulties; poor fixation; no cardiomyopathy; arched eye brows, synorphys; MRI brain 3m-38m no cerebellar atrophy (visual inspection); cerebellum not reduced in volume; no cerebellar hypoplasia; brainstem not reduced in volume; pons area not reduced in volume; no cerebral atrophy (visual inspection); cerebrum not reduced in volume ; no stroke-like abnormalities; no cystic degeneration of cerebellum; no cystic degeneration (noncerebellar); no basal ganglia involvement; no T2/FLAIR abnormalities white matter; delayed myelination; delayed myelination |
| Diagnosis/Initial |
neurodevelopmental delay |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
38m |
| Age/Diagnosis |
- |
| Age/Onset |
6d |
| Phenotype/Onset |
focal seizures |
| Protein |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-08-22 19:29:13 +02:00 (CEST) |
| Date last edited |
N/A |
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