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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Synthesis Lectures on Software Engineeringtion of steroids, whether glucocorticoids, mineralocorticoids or androgens and their precursors. With increasing dedifferentiation, the abnormal steroid output by tumours may not be detected by routine serum hormone assays, and therefore urine steroid profile can be invaluable for the identification

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Test Your Skills in C# ProgrammingThis introductory chapter presents a simple account of steroid structure, chemistry and nomenclature along with a description of relevant aspects of steroidogenesis and steroid metabolism. This introductory chapter provides a background for the disease specific chapters that follow.

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Test Your Skills in C# ProgrammingA brief review of adrenal physiology and steroidogenesis is given followed by a more comprehensive overview of adrenal pathophysiology. Inherited and acquired steroidogenic pathologies are described in the context of steroid excess and steroid deficiency.

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TestGoal and the Ten Test PrinciplesThe 11β-hydroxylase enzyme catalyses the final step in cortisol biosynthesis. Deficiency of the enzyme accounts for approximately 5% of cases of congenital adrenal hyperplasia and is characterised by virilisation, hypertension and an excessive output of urinary metabolites derived from the cortisol precursor, 11-deoxycortisol.

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Linda Makovická Osvaldová,Widya FatriasariCushing’s syndrome is the name given to a group of symptoms resulting from glucocorticoid excess. The majority of cases are the result of steroid administration, but pituitary, adrenal and ectopic causes also occur. The urine steroid profile is primarily useful for the investigation of adrenal Cushing’s syndrome.

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