1) congenital absence of thyroid gland
先天性甲状腺缺失
2) congenital absence of salivary gland
先天性涎腺缺失
3) congenital goiter
先天性甲状腺肿
4) congenital hypothyroidism
先天性甲状腺功能低下
1.
An association of mutations in thyroid transcription factor 1 gene with congenital hypothyroidism;
TTF-1基因突变与先天性甲状腺功能低下
2.
Objective To determine neonatal TSH level for diagnosing congenital hypothyroidism, and assessing neonatal iodine nutrition condition.
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。
3.
IntroductionCongenital hypothyroidism (CH) is a common neonatal metabolic disorder and may result in severe neurodevelopmental impairment.
研究背景 先天性甲状腺功能低下症(Congenital hypothyroidism,CH)是一种可导致严重智能发育落后的遗传代谢性疾病。
5) congenital hypothyroidism
先天性甲状腺功能减低
1.
Study of changes of serum insulin-like growth factor-1 and insulin-like growth factor binding protein-3 (IGFBP-3) in infants with congenital hypothyroidism;
先天性甲状腺功能减低患儿胰岛素样生长因子及其结合蛋白的变化
6) congenital atrophy of thyroid gland
先天性甲状腺萎缩
补充资料:先天性
先天性
congenitalness
不论其原因为何,凡出生时与生俱来或出生前所赋有的状况,均称为先天性。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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