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Prevalence (%) of clinical parameters based on data from 1 references describing 4 individuals
Add new symptom/sign to this disease
| Pubmed id number as a reference | Organ system affected | ||
| Number of patients in the reference | Percent affected patients (Between 0 and 1, eg. 0.1 = 10%) | ||
| Please provide your name and contact information as a reference | |||
| Name | Institute | Phone number | Email address |
List of symptoms
| Symptom/sign | Organ system | Percent affected | Pubmed id | Added on(yyyy-mm-dd) | Edit/add reference |
| Muscle weakness | nervous | 100 % | 9219740 | 2020-01-26 | |
| Muscle atrophy | nervous | 75 % | 9219740 | 2020-01-26 | |
| Neuropathy | nervous | 75 % | 9219740 | 2020-01-26 | |
| Foot ulcers | nervous | 50 % | 9219740 | 2020-01-26 | |
| Areflexia | nervous | 25 % | 9219740 | 2020-01-26 |
List of references:
Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.
P De Jonghe, V Timmerman, D FitzPatrick, P Spoelders, J J Martin, C Van Broeckhoven,
Journal of neurology, neurosurgery, and psychiatry - Jun 1997