Suppr超能文献

先天性甲状腺功能减退症。

Congenital Hypothyroidism.

机构信息

College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, Kingdom of Saudi Arabia.

出版信息

J Matern Fetal Neonatal Med. 2022 Oct;35(19):3761-3769. doi: 10.1080/14767058.2020.1838480. Epub 2020 Oct 28.

Abstract

Congenital hypothyroidism (CH) is the commonest preventable cause of mental retardation in human species. It is so important for clinician to know its etiology epidemiology, clinical manifestation and treatment strategies. Since it is one of the rare serious diseases that should not be diagnosed clinically because late clinical features corresponds to advanced mental retardation, the neonatal screening detection is the best and preferable way of early diagnosis of this congenital disease. Confirmatory laboratory and radiological diagnostic tests should be performed immediately after the positive neonatal screening test. In order to prevent mental defects and to maintain long term clinical as well as biochemical euthyroidism in affected children its diagnosis approach, medical treatment and follow-up should be well established knowledge to all pediatricians during the childhood period and later on to general practitioners when these individuals grow up as adults. Congenital hypothyroidism is a potentially serious disease that we need to emphasize on early detection, using proper diagnostic tools and early and planned therapeutic approach.

摘要

先天性甲状腺功能减退症(CH)是人类最常见的可预防智力障碍原因。临床医生了解其病因、流行病学、临床表现和治疗策略非常重要。由于它是一种罕见的严重疾病,不应该通过临床诊断,因为后期的临床特征与严重智力障碍相对应,因此新生儿筛查检测是早期诊断这种先天性疾病的最佳和首选方法。在新生儿筛查检测呈阳性后,应立即进行确认实验室和放射学诊断测试。为了预防智力缺陷并保持受影响儿童的长期临床和生化甲状腺功能正常,所有儿科医生在儿童期以及这些人长大后成为普通科医生时,都应该了解其诊断方法、治疗和随访。先天性甲状腺功能减退症是一种潜在的严重疾病,我们需要强调早期检测,使用适当的诊断工具,并进行早期和计划的治疗方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验