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Journal of the American Osteopathic Association, Vol 99, Issue 3, 165-165
Copyright © 1999 by American Osteopathic Association

Case Reports

Charcot-Marie-Tooth disease type I diagnosed in a 5-year-old boy after vincristine neurotoxicity, resulting in maternal diagnosis

MJ Olek, B Bordeaux, and RT Leshner

Charcot-Marie-Tooth disease type 1, also known as hereditary motor sensory neuropathy type 1, is an uncommon autosomal dominant disease that causes destruction of peripheral nerves with a varied clinical course, but often leads to muscle weakness. If the peroneal muscle is involved, the patient may develop a characteristic slapping gait. The dose-limiting side effect of the chemotherapeutic agent vincristine is usually its neurotoxicity. We report the case of a 5-year-old patient with leukemia who developed an acute polyneuropathy after treatment with vincristine. Charcot-Marie-Tooth disease type 1 was diagnosed in the patient and, subsequently, in his mother only after vincristine toxicity was observed.


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A. M. Orejana-Garcia, J. Pascual-Huerta, and A. Perez-Melero
Charcot-Marie-Tooth Disease and Vincristine
J Am Podiatr Med Assoc, May 1, 2003; 93(3): 229 - 233.
[Abstract] [Full Text] [PDF]




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Copyright © 1999 by the American Osteopathic Association.