1) pseudo-hypoparathyroidism
假性甲状旁腺功能低下
1.
ObjectiveTo improve the level of diagnosis of pseudo-hypoparathyroidism (PHP).
目的提高对假性甲状旁腺功能低下(P H P)症的认识和诊断水平。
2) hypoparathyroidism
[,haipəpærə'θairɔidizm]
甲状旁腺功能低下症
1.
Change of Blood Parathyroid Hormone Level in Hypoparathyroidism Treated by pcDNA3.1·PTH;
pcDNA3.1·PTH治疗甲状旁腺功能低下症血液甲状旁腺激素变化
2.
Objective To treat the patients of hypoparathyroidism caused by radical operation of thyroid carcinoma and to prevent recurrence of the cancer with combined transplantation of the whole thyroid parathyroid and thymus.
目的探讨联合移植甲状腺甲状旁腺及胸腺治疗甲状腺癌根治术后甲状旁腺功能低下症及预防甲状腺癌复发。
3) hypoparathyroidism
[,haipəpærə'θairɔidizm]
甲状旁腺功能低下
1.
A clinical analysis and prevention for hypoparathyroidism caused by total,subtotal thyroidectomy or second operation
甲状腺全次全切除或二次手术致甲状旁腺功能低下352例临床分析
2.
Analysis for CT diagnosis of brain of Hypoparathyroidism
甲状旁腺功能低下的颅脑CT诊断分析
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) Pituitary hypothyroidism
原发性甲状腺功能低下
6) hypothyroidism
[英][,haɪpəʊ'θaɪrɔɪdɪzəm] [美]['haɪpo'θaɪrɔɪ'dɪzəm]
甲状腺功能低下
1.
Effect of Hypothyroidism on Learning and Memory in Young Rats.;
甲状腺功能低下对幼年大鼠学习与记忆的影响
2.
Interview and Observation of 57 Cases With Congenital Hypothyroidism;
先天性甲状腺功能低下症57例随访观察
3.
The changes of BAEP in rats with hypothyroidism in the period of brain development;
脑发育期甲状腺功能低下大鼠脑干听觉诱发电位的变化
补充资料：甲状旁腺功能亢进症
甲状旁腺功能亢进症
hyperparath?yroidism
简称“甲旁亢”，甲状旁腺激素过多所致，可分原发性、继发性、三发性及假性四种。原发性甲旁亢，小儿不常见，因腺瘤或增生引起；继发性甲旁亢见于慢性肾功能不全、佝偻病等原因造成低血钙，刺激甲状旁腺代偿增生，使甲状旁腺分泌过多；三发性甲旁亢，是在继发性甲旁亢的基础上，由甲状旁腺代偿分泌过多变成自发性大量分泌；假性甲旁亢，是由某些恶性肿瘤分泌PTH样物质等。临床表现为高血钙综合征，神经肌肉的兴奋性降低，肌张力低下，肌肉软弱无力；消化功能降低，食欲不振、恶心、呕吐以及钙磷代谢紊乱等症状和体征；骨骼系统症状，持续性骨痛，病理性骨折等；泌尿系症状，如尿路结石、肾功能不全等。实验室检查，血钙增高，血磷降低，尿钙增多。本病主要以手术治疗为主。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条