先天性疼痛不敏感与无汗症(CIPA):第一例报告在孟加拉国

Mohammed Murad Hossain, Md Abdullah Yusuf
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摘要

先天性疼痛无汗不敏感症(CIPA)也被称为遗传性感觉和自主神经病变IV型。它是一种非常罕见的常染色体隐性遗传病,是由于周围神经的小髓鞘和无髓鞘纤维缺乏成熟而发生的。这些纤维是传递疼痛和温度感觉所必需的。这种疾病的特征是对疼痛不敏感,触觉完整,无汗,自残,反复出现不明原因的发烧,自动截肢,智力迟钝和;自婴儿期起自主神经系统异常。一名患有这种罕见疾病的4岁男孩的临床表现值得描述,这是孟加拉国报告的第一例病例。预防疾病并发症的康复治疗及其进展应在每次会议上得到重视。现代与先进医学研究杂志,2022年7月;9(2):91-94
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Congenital Insensitivity to Pain with Anhidrosis (CIPA): The First Reported Case in Bangladesh
Congenital insensitivity to pain with anhidrosis (CIPA) is also known as hereditary sensory and autonomic neuropathy type IV. It is an exceedingly rare autosomal recessive disease which occurs due to lack of maturation of small myelinated and unmyelinated fibers of peripheral nerves. These fibers are required for transmission of pain and temperature sensation. This disorder is characterized by insensitivity to pain with intact tactile perception, anhidrosis, self mutilation, recurrent unexplained fever, auto amputation, mental retardation & autonomic nervous system abnormality from infancy. The clinical presentation of a 4-year-old boy with this rare disease is worth to describe, as the first case to be reported in Bangladesh. Rehabilitative treatments for prevention of disease complications and their progress should be given emphasis in every encounter Journal of Current and Advance Medical Research, July 2022;9(2):91-94
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