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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease charcot-marie-tooth disease type 1a
Comorbidity C0029134|optic neuritis
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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