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PedAM

Pediatric Disease Annotations & Medicines




Disease charcot-marie-tooth disease
Symptom C0442874|neuropathy
Sentences 6
PubMedID- 23797954 Importance: no current medications improve neuropathy in subjects with charcot-marie-tooth disease type 1a (cmt1a).
PubMedID- 21274281 This demonstrates a rather different phenotype, referred to as charcot-marie-tooth disease type 1a with demyelinating neuropathy .
PubMedID- 26376783 Furthermore, in humans, mutations in mitochondrial genes frequently result in the development of painful peripheral neuropathy, as seen in patients with charcot-marie-tooth disease 6.
PubMedID- 22900182 Patients were excluded if they had concomitant foot ulcer, orthopaedic or surgical problems influencing gait parameters, a nondiabetic neuropathy (due to charcot-marie-tooth disease, alcohol, or thyroid dysfunction), or neurological pathology influencing gait parameters.
PubMedID- 23197742 Compound charcot-marie-tooth disease: a kindred with severe hereditary neuropathy, pupil abnormalities and a novel mpz mutation.
PubMedID- 22996176 Corneal confocal microscopy detects small-fiber neuropathy in charcot-marie-tooth disease type 1a patients.

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