PedAM
Pediatric Disease Annotations & Medicines
| Disease | tooth disease |
| Phenotype | C0442874|neuropathy |
| Sentences | 7 |
| PubMedID- 22996176 | Corneal confocal microscopy detects small-fiber neuropathy in charcot-marie-tooth disease type 1a patients. |
| 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- 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- 19921145 | Exclusion criteria were: patients with concomitant foot ulcers, orthopaedic or surgical problems affecting gait variables, non-diabetic neuropathy (due to charcot–marie–tooth disease or alcohol), other neurological pathologies (other than peripheral neuropathy) that could influence gait variables or inability to walk a minimum of 500 m without a walking aid.training programmes started as soon as enough patients (20 to 28 per group) had been recruited, i.e. |
| PubMedID- 23197742 | Compound charcot-marie-tooth disease: a kindred with severe hereditary neuropathy, pupil abnormalities and a novel mpz mutation. |
| PubMedID- 23797954 | Importance: no current medications improve neuropathy in subjects with charcot-marie-tooth disease type 1a (cmt1a). |
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