| 先天性甲状腺功能减低症诊疗共识 |
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| 引用本文： | Subspecialty Group of Endocrinologic, Hereditary and Metabolic Diseases, The Society of Pediatrics, Chinese Medical Association;Group for Newborn Screening, Society of Child Health, Chinese Preventive Medicine Association. 先天性甲状腺功能减低症诊疗共识[J]. 中华儿科杂志, 2011, 49(6): 421-424. DOI: 10.3760/cma.j.issn.0578-1310.2011.06.006 |
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| 作者姓名： | Subspecialty Group of Endocrinologic, Hereditary and Metabolic Diseases, The Society of Pediatrics, Chinese Medical Association Group for Newborn Screening, Society of Child Health, Chinese Preventive Medicine Association |
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| 摘 要： | ![]()
前言先天性甲状腺功能减低症(congenital hypothyroidism,简称先天性甲低)是引起儿童智力发育及体格发育落后的常见小儿内分泌疾病之一,也是可预防、可治疗的疾病.由于先天性甲低患儿在新生儿期可无特异性临床症状或者症状轻微,对新生儿进行群体筛查是早期发现先天性甲低的主要方法.我国自1981年开始进行新生儿先天性甲低的筛查,目前全国筛查覆盖率已经超过60%,发病率约为1/2050[1-4].随着新生儿疾病筛查在全国范围的进一步推广,进行先天性甲低诊治的医疗机构和专科医师不断增多.为规范疾病的诊断和治疗,2010年卫生部颁布了<新生儿疾病筛查技术规范(2010版)>[5].本文在此规范框架基础上,针对先天性甲低的新生儿筛查、筛查结果分析、诊断和处理、随访等环节,提出进一步的操作共识.
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Consensus statement on the diagnosis and management of congenital hypothyroidism |
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| Subspecialty Group of Endocrinologic, Hereditary and Metabolic Diseases, The Society of Pediatrics, Chinese Medical Association;Group for Newborn Screening, Society of Child Health, Chinese Preventive Medicine Association. Consensus statement on the diagnosis and management of congenital hypothyroidism[J]. Chinese journal of pediatrics, 2011, 49(6): 421-424. DOI: 10.3760/cma.j.issn.0578-1310.2011.06.006 |
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| Authors: | Subspecialty Group of Endocrinologic, Hereditary Metabolic Diseases, The Society of Pediatrics, Chinese Medical Association Group for Newborn Screening, Society of Child Health, Chinese Preventive Medicine Association |
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| Abstract: | ![]()
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