先天性甲状腺功能低下

目的对6590例新生儿于生后72小时进行先天性甲状腺功能低下的筛查，做到早期诊断、早期治疗。

Objective To screen the congenital hypothyroidism from neonates , so that early stage diagnosis and treatment .

TTF-1基因突变与先天性甲状腺功能低下

An association of mutations in thyroid transcription factor 1 gene with congenital hypothyroidism

目的：探讨重庆市新生儿先天性甲状腺功能低下症（CH）的发生率和治疗效果。

Objective : To explore the incidence of neonatal congenital hypothyroidism in Chongqing and the effect of treatment on it .

目的通过检测新生儿促甲状腺激素（TSH）水平，诊断先天性甲状腺功能低下症，评价西安市新生儿碘营养状况。

Objective To determine neonatal TSH level for diagnosing congenital hypothyroidism , and assessing neonatal iodine nutrition condition .

目的：报告先天性甲状腺功能低下症（CH）和苯丙酮尿症（PKU）的患病率。

Objective To describe the incidence of congenital hypothyroidism ( CH ) and phenylketonuria ( PKU ) in Maanshan city .

本文报告采用TSH干血滴纸片放射免疫分析法筛查先天性甲状腺功能低下症。

The method of screening for congenital hypothyroidism using radioimmunoassay ( RIA ) of thyroid-stimulating hormone ( TSH ) in dried blood spot was reported in this study .

先天性甲状腺功能低下及苯丙酮尿症的治疗早晚的ABR对比观察，可作为疗效随访和追踪观察的客观指标。

The comparison of ABR changes at the beginning of therapy against congenital hypothyroidism and phenylketonuria and later could serve as an objective criteria for follow-up of therapeutic efficiency .

结果4例先天性甲状腺功能低下症患儿NHI分值平均5.6（范围3.8～8.0）；

M. Results NHI were determined averaged 5.6 ( from 3.0 ~ 8.0 ) in 4 patients with Congenital Hypothyroidism .

目的探讨新生儿先天性甲状腺功能低下症（CH）筛查的检测方法，新生儿出生季节对碘营养状况正常的新生儿足跟血促甲状腺激素（TSH）测定值的影响。

[ Objective ] To explore the testing method for CH screening and the influence of birth season on the TSH level in the heel blood of the neonates who had normal iodine nutrition .

结论：TRFIA法筛查新生儿先天性甲状腺功能低下症（CH）干血纸片TSH值精密度高，能有效进行质量监控。

Conclusions : The precision of the TSH testing value in dried blood spots tested by TRFIA to screen newborn Congenital Hypothroidism ( CH ) is high and the quality can be controlled effectively .

测定脐血清促甲状腺激素水平筛选新生儿先天性甲状腺功能低下

Screening Survey of Neonatal Congenital Hypothyroidism by Umbilical Serum TSH Determination

浙江省1999-2004年新生儿先天性甲状腺功能低下症筛查分析

Screening for congenital hypothyroidism in neonates of Zhejiang Province during 1999-2004

初始小剂量L-甲状腺素治疗先天性甲状腺功能低下症疗效研究

Low initial dose of levothyroxine for treatment of congenital hypothyroidism

先天性甲状腺功能低下症57例随访观察

Interview and Observation of 57 Cases With Congenital Hypothyroidism

韶关市新生儿先天性甲状腺功能低下症筛查

Analysis of Neonatal Screening for Congenital Hypothyroidism in Shaoguan

重庆市新生儿先天性甲状腺功能低下症的筛查结果分析

Analysis on the results of congenital hypothyroidism screening in the newborn infants of Chongqing

对先天性甲状腺功能低下症患儿家长实施健康教育的初步探讨

Preliminary study on carrying out health education on the genearch of children with congenital hypothyroidism

先天性甲状腺功能低下的新生儿筛查

Neonatal screening for congenital hypothyroidism

儿童先天性甲状腺功能低下由甲状腺发育不良或甲状腺激素合成障碍引起。

Primary congenital hypothyroidism ( CH ) is caused by thyroid dysgenesis or by the disturbance of thyroid hormone synthesis .

辽宁阜新农村地区高血压发病率及其危险因素新生儿先天性甲状腺功能低下症的危险因素

Incidence and Predictors of Hypertension among Rural Chinese Adults : Results from Liaoning Province Risk factors for congenital hypothyroidism in newborn

脐血清检测T4TSH筛查先天性甲状腺功能低下及影响因素的探讨

A study of the Effect of Detecting T_4 , TSH in the Cord Blood Serum on Selecting and Identifying Patients With Congenital Hypothyrosis

目的建立长沙地区新生儿先天性甲状腺功能低下症促甲状腺素筛查的切值。

Objective To determine cut-off value of thyrotropin ( TSH ) for screening of congenital hypothyroidism ( CH ) of newborn in Changsha city , Hunan province .

治疗苯丙酮尿症特异性药物二盐酸沙丙蝶呤新生儿先天性甲状腺功能低下症和苯丙酮尿症的筛查与疗效评估

A specific drug to treat PKU : sapropterin dihydrochloride EVALUATION OF THERAPEUTIC EFFECT AND SCREENING FOR CONGENITAL HY-POTHYROIDISM ( CH ) AND PHENYLETONURIA ( PKU ) IN NEONATES

结论新生儿足跟血促甲状腺素切值的确定为长沙地区今后开展大规模的新生儿先天性甲状腺功能低下症筛查提供了依据。

Conclusion The determination of TSH cut-off value of newborn provides a basis for large scale screening of congenital hypothyroidism ( CH ) among the newborns in Changsha city .

随访资料显示婴儿染色体异常2例、先天性甲状腺功能低下1例、粒细胞减少症1例、白化病1例、不明原因死亡5例。

Follow-up on the baby donors showed two cases with chromosome abnormality , one with hypothyroidism , one with neutropenia , one with albinism and 5 dead with unclear reasons .

先天性原发性甲状腺功能低下的~（99m）Tc甲状腺γ显像

~ ( 99m ) tc for detection of thyroid tissue in congenital primary hypothyroidism