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一名反复出现角膜溃疡的儿童:遗传性感觉和自主神经病变IV型(HSAN IV)

A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV).

作者信息

Suresh Beena, Reddy Vaishnavi, Kurth Ingo, Jagadeesh Sujatha

机构信息

Department of Clinical Genetics, Mediscan Systems, Chennai, India.

Institut für Humangenetik, der RWTH Aachen, Germany.

出版信息

Neuroophthalmology. 2018 Aug 22;43(5):310-312. doi: 10.1080/01658107.2018.1506937. eCollection 2019 Nov.

Abstract

Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV) or Congenital Insensitivity to pain and Anhidrosis is an autosomal recessive condition. It is characterized by absence of reaction to painful stimuli, anhidrosis, self-mutilating behaviour and episodic fever. We report a child with HSAN IV who presented primarily with recurrent corneal ulcers and the classical history helped us clinch the diagnosis. Molecular testing revealed a homozygous pathogenic frameshift mutation in c.717delG, p.(Met239fs). Molecular testing is confirmatory and this will help the family in future prenatal diagnosis.

摘要

遗传性感觉和自主神经病变IV型(HSAN IV)或先天性无痛觉伴无汗症是一种常染色体隐性疾病。其特征为对疼痛刺激无反应、无汗、自残行为和间歇性发热。我们报告了一名患有HSAN IV的儿童,该患儿主要表现为复发性角膜溃疡,典型的病史帮助我们确诊。分子检测显示在c.717delG,p.(Met239fs)处存在纯合致病性移码突变。分子检测具有确诊作用,这将有助于该家庭未来的产前诊断。

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