Two sisters with a Charcot-Marie-Tooth disease type 1A (CMT1A) duplication, who had an unusual CMT1A clinical phenotype, are described. The 63-year-old proband presented with dysesthesia on the inner side of the right leg. Neurological examination revealed a localized sensory disturbance in the lowe
Delayed neurophysiologic abnormalities in Charcot–Marie–Tooth disease type 1A
✍ Scribed by Monique M. Ryan; H. Royden Jones Jr.
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 53 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0148-639X
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