PedAM
Pediatric Disease Annotations & Medicines
| Disease | optic neuritis |
| Phenotype | C0007959|charcot-marie-tooth disease |
| Sentences | 1 |
| PubMedID- 21764587 | We report the development of sequential demyelinating optic neuritis in a patient with genetically confirmed charcot-marie-tooth disease type 1a, a hereditary neuropathy. |
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