Clinical and neurophysiological investigation of a large family with dominant Charcot-Marie-Tooth type 2 disease with pyramidal signs

Arquivos de Neuro-Psiquiatria

Eduardo Luis De Aquino Neves²  Fernando Kok¹ 

[1] ,University of São Paulo Department of Neurology São Paulo SP ,Brazil

关键词: Charcot-Marie-Tooth disease;    CMT2;    axonal hereditary neuropathy;    doença de Charcot-Marie-Tooth;    CMT2;    neuropatia hereditária axonal;   

DOI  :  10.1590/S0004-282X2011000400003

来源: SciELO

【 摘 要 】

Charcot-Marie-Tooth (CMT) disease is a hereditary neuropathy of motor and sensory impairment with distal predominance. Atrophy and weakness of lower limbs are the first signs of the disease. It can be classified, with the aid of electromyography and nerve conduction studies, as demyelinating (CMT1) or axonal (CMT2). OBJECTIVE: Clinical and neurophysiological investigation of a large multigenerational family with CMT2 with autosomal dominant mode of transmission. METHOD: Fifty individuals were evaluated and neurophysiological studies performed in 22 patients. RESULTS: Thirty individuals had clinical signs of motor-sensory neuropathy. Babinski sign was present in 14 individuals. Neurophysiological study showed motor-sensory axonal polyneuropathy. CONCLUSION: The clinical and neurophysiological characteristics of this family does not differ from those observed with other forms of CMT, except for the high prevalence of Babinski sign.

【 授权许可】

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