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. |
Page: 1