先天性无痛无汗症研究进展  

Research on the Progress of Congenital Insensitivity to Pain With Anhidrosis

作　　者：刘世祺 吴琳[2] 张保贵[1] 靳猛[1] 郭东立[1] LIU Shiqi WU Lin ZHANG Baogui JIN Meng GUO Dongli(Department of Gastrointestinal, The Affiliated Hospital of Ji＇ning Medical College, Jining Shandong 272029, China Intensive Care Unit)

机构地区：[1]济宁医学院附属医院胃肠外科,山东济宁272029 [2]济宁医学院附属医院重症监护室二区,山东济宁272029

出　　处：《中国继续医学教育》2017年第17期157-159,共3页China Continuing Medical Education

摘　　要：先天性无痛无汗症在临床上又被称为遗传性感觉和自主神经障碍IV型,是一种罕见遗传性疾病。先天性无痛无汗症的主要临床表现为痛觉丧失,温度感觉减低或者丧失,全身无汗,皮肤干燥、发热症状。本文主要介绍了先天性无痛无汗症的发病机制、主要症状、诊断方法以及相关的治疗措施,并对近年来关于先天性无痛无汗症的研究进展进行介绍。Congenital insensitivity to pa!n with anhidrosis is clinically known as hereditary sensory and autonomic neuropathy, and IV is a rare genet!c disease. The main clinical manifestations of congenital insensitivity to pain with anhidrosis include loss of pain, loss of temperature sensation, loss of the whole body, sweating, dry skin and fever. This article mainly introduces the pathogenesis, main symptoms, diagnosis methods and related treatment measures of congenital insensitivity to pain with anhidrosis, and introduces the research progress of congenital painless non-hyperhidrosis in recent years.

关 键 词：先天性无痛无汗症 发病机制 临床症状 诊断 研究进展 

分 类 号：R726[医药卫生—儿科]