eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | charcot-marie-tooth disease |
| Comorbidity | C0442874|neuropathy |
| Sentences | 6 |
| PubMedID- 21274281 | This demonstrates a rather different phenotype, referred to as charcot-marie-tooth disease type 1a with demyelinating neuropathy [11–13]. |
| 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. |
| PubMedID- 23797954 | Importance: no current medications improve neuropathy in subjects with charcot-marie-tooth disease type 1a (cmt1a). |
| PubMedID- 21252112 | charcot-marie-tooth disease type 1a is a hypertrophic de-remyelinating neuropathy manifesting with peroneal muscular atrophy and uniform, marked, slowing of nerve conduction velocities. |
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