Chronic peripheral neuropathy in childhood: an overview.

Australian paediatric journal Pub Date : 1988-01-01
R A Ouvrier, J G McLeod
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Abstract

One hundred and twenty-five cases of biopsy-proven subacute or chronic peripheral polyneuropathy occurring in children under 17 years of age are reviewed. Ninety-three (74%) of the cases have been examined by the authors. At least 71% of cases were considered to be of genetic origin. Hereditary motor and sensory neuropathies were confirmed in over 40% of the cases. From among these a previously poorly defined entity (hereditary motor and sensory neuropathy of neuronal type with onset in early childhood) was delineated. It constituted 7.2% of the cases. When clinical and neurophysiological investigations of the family are combined with histopathological investigation of the affected child, a correct aetiological diagnosis can be reached in over 80% of cases of chronic polyneuropathy in childhood.

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儿童慢性周围神经病变:综述。
125例活检证实亚急性或慢性周围多神经病变发生在17岁以下的儿童回顾。93例(74%)病例已由作者检查。至少71%的病例被认为是遗传原因。遗传性运动和感觉神经病变在40%以上的病例中得到证实。从这些以前不明确的实体(遗传性运动和感觉神经病变神经元型发病早期儿童)被划定。占案件总数的7.2%。当家庭的临床和神经生理调查与患病儿童的组织病理学调查相结合时,超过80%的儿童慢性多发性神经病病例可以达到正确的病因诊断。
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