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由于DUOXA2基因突变导致的持续性甲状腺肿伴先天性甲状腺功能减退症。

Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene.

作者信息

Jung So Yoon, Lee Jeongho, Lee Dong Hwan

机构信息

Department of Pediatrics, Soonchunhyang University Seoul Hospital, Seoul, Korea.

出版信息

Ann Pediatr Endocrinol Metab. 2020 Mar;25(1):57-62. doi: 10.6065/apem.2020.25.1.57. Epub 2020 Mar 31.

Abstract

Thyroid hormones are crucial for development of the central nervous system. Congenital hypothyroidism (CH) is the most common preventable disease resulting in mental retardation. A neonatal screening test (NST) can detect a mild form of CH that can be treated at an early age. Generally after 3 years of age, when most of the brain has matured, clinicians consider reevaluation of thyroid function for CH patients that have been identified with a normal thyroid gland at a normal position. This report presents three CH patients that developed normally, with persistent goiter despite thyroid hormone supplements. The patients' initial thyroid-stimulating hormone (TSH) level after NST was 47, 157, and 57 mIU/L, respectively. Levothyroxine administration began at 1 or 2 months of age and was terminated after reevaluation at the age of 3, 15, and 5 years, respectively. However, 1 or 2 years later, they all resumed their medication due to increased TSH level coupled with newly developed or enlarged goiter. They all showed dual oxidase maturation factor 2 (DUOXA2) gene mutation: a homozygous mutation with DUOXA2 (c.413dupA; p.Tyr138*) in case 1, a presumed compound heterozygotic mutation with DUOXA2 (p.Tyr138*/p.Tyr246*) in case 2, and heterozygous mutations with DUOXA2 (c.738C>G; p.Tyr246*) and TPO (c.2268dupT; p.Glu757*) in case 3. When goiter persists or is newly developed despite a maintained euthyroid status, for those with transient CH history, follow-up to assess the thyroid function is recommended for at least 1 or 2 years, and genetic testing would be helpful. This study presents the first clinical cases of DUOXA2 mutation in Korea.

摘要

甲状腺激素对中枢神经系统的发育至关重要。先天性甲状腺功能减退症(CH)是导致智力发育迟缓的最常见可预防疾病。新生儿筛查试验(NST)可检测出可在幼年时治疗的轻度CH形式。一般在3岁以后,当大部分大脑已经成熟时,临床医生会考虑对在正常位置甲状腺正常的CH患者重新评估甲状腺功能。本报告介绍了3例发育正常但尽管补充了甲状腺激素仍持续存在甲状腺肿的CH患者。患者在NST后的初始促甲状腺激素(TSH)水平分别为47、157和57 mIU/L。左甲状腺素给药分别在1或2个月龄开始,并在3岁、15岁和5岁重新评估后终止。然而,1或2年后,由于TSH水平升高以及新出现或增大的甲状腺肿,他们都恢复了用药。他们均显示双氧化酶成熟因子2(DUOXA2)基因突变:病例1为DUOXA2纯合突变(c.413dupA;p.Tyr138*),病例2为推测的DUOXA2复合杂合突变(p.Tyr138*/p.Tyr246*),病例3为DUOXA2杂合突变(c.738C>G;p.Tyr246*)和甲状腺过氧化物酶(TPO)杂合突变(c.2268dupT;p.Glu757*)。对于有短暂性CH病史且尽管维持甲状腺功能正常但甲状腺肿持续存在或新出现的患者,建议至少随访1或2年以评估甲状腺功能,基因检测可能会有帮助。本研究展示了韩国首例DUOXA2突变的临床病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c7a/7136507/8b43305a4cc6/apem-2020-25-1-57f1.jpg

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