congenital adrenal hyperplasiaandrogen excess symptomsmolecular basis of CAHA clinical spectrum, varying from prenatal onset to postnatal onset of symptoms, exists in all hyperandrogenic forms of congenital adrenal hyperplasia (CAH). Postnatal onset hyperandrogenic symptoms such as premature pubarche, clitor...
Congenital adrenal hyperplasia (CAH) is a group of inherited diseases that result from a deficiency of one or more of the enzymes required for cortisol and aldosterone synthesis in the adrenal cortex. CAH is the most common genetic endocrine disorder in humans, and the hormonal abnorm...
With normalization of progestins, menses began or resumed in these cases.We conclude: 1) control of progestin levels, particularly 17P, is impossible on standard forms of therapy in some cases of CAH, 2) this is occasionally due to occult mineralocorticoid deficiency, 3) low-dose dex is the...
Congenital adrenal hyperplasia (CAH) refers to a family of inherited disorders of adrenal steroidogenesis. The common functional defect in each disorder is impaired cortisol secretion, resulting in hypersecretion of corticotropin-releasing hormone (CRH) and adrenocorticotropic hormone (ACTH) and consequent ...
名词解释 先天性肾上腺皮质增生症(congenitaladrenalhyperplasiaCAH) 答案: 是一组由于肾上腺皮质激素合成过程中酶的缺陷所引起的疾病,属常染色体隐性遗传病。点击查看答案 手机看题 你可能感兴趣的试题 名词解释 单纯乳房早发育 答案: 是女孩不完全性性早熟的表现。起病年龄小,常小于2岁,乳腺仅轻度发育,且常呈...
Bongiovanni, A. M., Unusual steroid pattern in congenital adrenal hyperplasia: deficiency of 3β-hydroxy-dehydrogenase,J. Clin. Endocrinol.21:860 (1961). CASGoogle Scholar Bongiovanni, A. M., The adrenogenital syndrome with deficiency of 3β-hydroxy-steroid dehydrogenase,J. Clin. Invest.41:2086...
CongenitalAdrenalHyperplasiadueto 21-HydroxylaseDeficiency* PERRINC.WHITEANDPHYLLISW.SPEISER DivisionofPediatricEndocrinology(P.C.W.),UniversityofTexasSouthwesternMedicalCenter, Dallas,Texas75390-9063;andDivisionofPediatricEndocrinology(P.W.S.),NorthShoreUniversity ...
摘要: Congenital adrenal hyperplasia (CAH) refers to a family of inherited disorders of adrenal steroidogenesis. The common functional defect in each disorder is impaired cortisol secretion, resulting in hyDOI: 10.1007/978-1-4939-2401-1_48 年份: 2017 ...
The pituitary-adrenal axis and the renin-angiotensin system in treated congenital adrenal hyperplasia41 out-patients, treated for 21-hydroxylase deficiency with oral cortisol (15 mg-30 mg/m2), were studied at regular intervals. Among them were 24 salt-losers, who, in addition to cortisol,...
congenital adrenal hyperplasiaandrogen excess symptomsmolecular basis of CAHPediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of diseases of children and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in ...