先天性肾上腺皮质增生症

报告4例儿童21-羟化酶缺陷型先天性肾上腺皮质增生症。

Four cases of defects in 21-hydroxylation of congenital hyperplasia have been reported .

【医】婴儿骨外层肥厚症先天性肾上腺皮质增生症患儿家长的健康教育需求研究

Study on parents ' demands on health education of children with congenital adrenal hyperplasia

雄激素拮抗剂氟他胺在先天性肾上腺皮质增生症治疗中应用探索

Pilot study on application of antiandrogen ( flutamide ) in the treatment of congenital adrenal hyperplasia

目的在上海地区新生儿疾病筛查项目中调查先天性肾上腺皮质增生症的发病率。

Objective To investigate the incidence of congenital adrenal hyperplasia ( CAH ) in Shanghai areas by a neonatal screening program .

目的探讨先天性肾上腺皮质增生症21羟化酶缺陷的产前诊断方法。

Objective To explore the method for prenatal diagnosis of congenital adrenal hyperplasia ( CAH ) with 21-hydroxylase deficiency ( 21-OHD ) .

另外5例为早产原因所致17OHP升高。结论干血滤纸片法测定17羟孕酮适用于大规模开展先天性肾上腺皮质增生症筛查。

Conclusions Determining 17 OHP level on dried blood spotted filter paper is a reliable and practical approach for CAH mass screening in neonates .

本文报道一例先天性肾上腺皮质增生症（11&β-羟化酶缺乏）的女性患者，并对本症的临床、诊断及治疗进行了讨论。

Here reported is a female pseudohermaphroditism due to 11 - β - hydroxylase deficit . Its clinical forms , diagnosis and treatment were discussed .

最常见的原因是先天性肾上腺皮质增生症引起的性别的模棱两可，内分泌紊乱的情况下，肾上腺产生水平高得异常的激素。

The most common cause of sexual ambiguity is congenital adrenal hyperplasia , an endocrine disorder where the adrenal glands produce abnormally high levels of hormones .

目的开展新生儿先天性肾上腺皮质增生症筛查，降低残疾儿童的发生率，提高人口素质。

Objective To develop the neonatal screening for congenital adrenal hyperplasia in order to prevent children from congenital disability and improve the aristogenesis in our country .

McCune-Albright综合征5例，卵巢囊肿2例，卵巢颗粒细胞瘤、先天性肾上腺皮质功能增生症各1例。

Cases of wrong contraceptive intake were 29,5 cases of McCune-Albright syndrome , 2 cases of ovarian cyst , 1 case of ovarian granular cell tumor , 1 case of congenital adrenal hyperplasia .