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- contenital adrenal hyperplasia 先天性肾上腺增生症, 类固醇-羟化酶缺乏症
- Congenital adrenal hyperplasia is a genetic disorder transmitted by autosomal recessive pattern. 摘要先天性肾上腺增生症是一种自体隐性遗传病。
- Adrenal Hyperplasia, adrenal adenoma and pheochromocytoma are the more common cause of adrenal-derived hypertension. 肾上腺增生、肾上腺腺瘤和嗜铬细胞瘤是较常见引起肾上腺源性高血压的病因。
- Objective To explore the method for prenatal diagnosis of congenital adrenal hyperplasia (CAH) with 21-hydroxylase deficiency (21-OHD). 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。
- In fact, congenital adrenal hyperplasia or earlyadministration of diethylstilbestrol are able to modify female play behavior in mammals. 实际上，先天性肾上腺皮质增生或进行早期投药(己烯雌酚)都会改变雌性哺乳动物的游戏行为。
- Testicular tumor of adrenogenital syndrome, also being called adrenal rests, is rare bilateral intratesticular tumors highly associated with congenital adrenal hyperplasia (CAH). 摘要睪丸的肾上腺遗迹是很罕见的双侧睪丸内肿瘤，而且和先天性肾上腺增生有高度的相关性。
- The most common cause of sexual ambiguity is congenital adrenal hyperplasia, an endocrine disorder where the adrenal glands produce abnormally high levels of hormones. 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。
- We recommend that patients with bilateral adrenal hyperplasia, or those unsuitable for surgery, optimally be treated medically by mineralocorticoid receptor antagonists. 在每个阶层的推荐中，特别委员会小组都撰写了专门的注解及内部需要的变化。
- This male-pattern hair loss is often seen in women with polycystic oary syndrome (PCOS), congenital adrenal hyperplasia, and other disorders of male hormone excess. 这种男型脱发常见于PCOS女性、先天性肾上腺增生和其它男性激素过剩相关疾病。
- Conclusions Patients with congenital adrenal hyperplasia and CPP were closely related to the advanced bone age,earlier diagnosis and treatment could improve the prog-nosis. 结论CAH患儿骨龄发育提前是发生性早熟的主要原因,早诊断和早治疗可改善预后。
- This lesion accounts for about two-thirds of cases of primary hyperaldosteronism (PHA), while bilateral adrenal hyperplasia accounts for about 30% of PHA. 这种病变占原发性醛固酮增多症（PHA）的2/3，而双侧肾上腺增生占PHA的30%25。
- Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency. 结论羊水细胞DNA分析是先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断的可靠方法。
- The CPP occurred at2.3years after treatment with hydrocortisone in group B.Conclusions Patients with congenital adrenal hyperplasia and CPP were closely related to the advanced bone age,earlier diagnosis and treatment could improve the prog-nosis. B组应用氢化可的松治疗后平均2.;3年出现中枢性性早熟。 结论CAH患儿骨龄发育提前是发生性早熟的主要原因;早诊断和早治疗可改善预后。
- Studies suggest that OCP treatment does increase insulin resistance, which is not only present in PCOS, but to some extent in other androgen excess diseases such as congenital adrenal hyperplasia. 研究显示口服避孕药的确可以增大胰岛素抵抗，胰岛素抵抗不仅存在于PCOS中，也存在于其它雄激素过剩的疾病中，如先天性肾上腺增生。
- Methods Clinical and follow up data were summarized for 42 children with adrenogenital syndrome, including 30 cases of congenital adrenal hyperplasia (CAH) and 12 cases of adrenal cortex tumor. 方法总结42例小儿肾上腺性征异常症的临床资料,其中先天性肾上腺皮质增生(CAH)30例,肾上腺皮质肿瘤12例。
- Objective To st ud y the characteristics of clinical manifestations and laboratory findings in pati ents with adrenocorticotropin-independent macronodular adrenal hyperplasia (AIM AH). 目的探讨非ACTH依赖性双侧肾上腺皮质大结节增生症(AIMAH)的临床特点。
- Diagnosis of non salt-losing type congenital adrenal hyperplasia due to 21-hydroxylase dcficiency in male is always delayed until the patient presents with precocious pseudopuberty. 临床表现可因患者性别及酵素缺乏的种类及程度而不同。
- congenital adrenal hyperplasia(CAH) 先天性肾上腺皮质增生症
- congenital lipoid adrenal hyperplasia 先天性肾上腺类脂组织增生
- congenital virilizing adrenal hyperplasia 先天性男性化肾上腺增生, 肾上腺(性)性征综合征
