PedAM
Pediatric Disease Annotations & Medicines
| Disease | n syndrome |
| Phenotype | C0004134|ataxia |
| Sentences | 2 |
| PubMedID- 24028880 | Childhood ataxia with cerebral hypomyelination syndrome: a variant of patient with early childhood onset related to eif2b3 mutation. |
| PubMedID- 22849991 | His sensory ataxia might be attributed to sjogren syndrome-associated ganglionopathy at the cervical level, and the mri findings might reflect centripetal wallerian degeneration in the cuneate fasciculus. |
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