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先天性无痛觉伴无汗症:一例报告

Congenital insensitivity to pain with anhidrosis: a case report.

作者信息

Kim J S, Woo Y J, Kim G M, Kim C J, Ma J S, Hwang T J, Lee M C

机构信息

Department of Pediatrics, Chonnam National University Medical School, Kwangju, Korea.

出版信息

J Korean Med Sci. 1999 Aug;14(4):460-4. doi: 10.3346/jkms.1999.14.4.460.

Abstract

Congenital insensitivity to pain with anhidrosis (CIPA) is a very rare genetic disorder of the peripheral nervous system characterized by recurrent episodes of unexplained fever, generalized anhidrosis, insensitivity to pain and temperature, and accompanied by self-mutilating behavior and mental retardation. We report on a 16 month-old boy with CIPA who exhibited these characteristic clinical features. A sural nerve biopsy revealed markedly reduced numbers of unmyelinated and small myelinated fibers, consistent with the characteristic features of CIPA.

摘要

先天性无痛无汗症(CIPA)是一种非常罕见的外周神经系统遗传性疾病,其特征为不明原因发热反复发作、全身性无汗、对疼痛和温度不敏感,并伴有自残行为和智力发育迟缓。我们报告了一名患有CIPA的16个月大男孩,他表现出了这些典型的临床特征。腓肠神经活检显示无髓鞘和小髓鞘纤维数量明显减少,与CIPA的特征相符。

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