Titlebook: Disorders of Steroidogenesis; Guide to Steroid Pro Gill Rumsby,Gary M. Woodward Book 2019 Springer International Publishing AG, part of Spr

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書目名稱Disorders of Steroidogenesis影響因子(影響力)




書目名稱Disorders of Steroidogenesis影響因子(影響力)學(xué)科排名




書目名稱Disorders of Steroidogenesis網(wǎng)絡(luò)公開度




書目名稱Disorders of Steroidogenesis網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Disorders of Steroidogenesis被引頻次




書目名稱Disorders of Steroidogenesis被引頻次學(xué)科排名




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書目名稱Disorders of Steroidogenesis讀者反饋學(xué)科排名

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Automatische Generierung von Testdaten,ital adrenal hyperplasia. The disorder is characterised by a variable degree of renal salt-losing caused by aldosterone insufficiency and virilisation as a result of exposure to excess androgens produced in utero and after birth in untreated patients. Urine steroid profiles allow early diagnosis and

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AORTA

Ping Du,Maoke Chen,Akihiro Nakaoen synthesis in the male and is a cause of 46XY disorder of sex development. Overproduction of steroids with mineralocorticoid properties can lead to low renin hypertension in both sexes. The urine steroid profile is characterised by excess progesterone and corticosterone metabolites.

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Testen von Informationssystemenongenital adrenal hyperplasia (CAH) characterised by a complete or partial inability of the adrenal glands to synthesise glucocorticoids, mineralocorticoids and adrenal androgens. Low levels of their respective metabolites are therefore observed in the urine steroid profiles of patients with either

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Neutrinos Within the Standard Modelan present with a salt-losing crisis in infancy. Patients surviving this period may be asymptomatic in adulthood. Aldosterone synthase deficiency is inherited as an autosomal recessive trait due to loss of function mutations in ., and it is extremely rare. The characteristic biochemical features are

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Neutrinos Within the Standard Modelof the oxygen moiety at C17 of the steroid molecule. Deficiency of the type 3 enzyme leads to a disorder of sex development through failure of testicular androgen production - a similar phenotype to androgen insensitivity and 5α-reductase deficiency. Biochemical diagnosis can be made by measurement

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