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A 5 year old boy developed severe weakness after receiving vincristine for treatment of acute lymphoblastic leukaemia. Although weakness improved after the discontinuation of vincristine, other symptoms suggestive of a neuropathy persisted. Neurophysiological and genetic analysis at age 8 years indicated that vincristine had induced symptoms of a hereditary sensory motor neuropathy type 1A, which had previously been asymptomatic; his genetically affected mother was also asymptomatic.

More information Original publication

DOI

10.1136/adc.81.5.442

Type

Journal article

Publication Date

1999-11-01T00:00:00+00:00

Volume

81

Pages

442 - 443

Total pages

1

Keywords

Antineoplastic Agents, Phytogenic, Charcot-Marie-Tooth Disease, Child, Preschool, Follow-Up Studies, Humans, Male, Vincristine