Literature DB >> 26038201

Adrenal steroidogenesis and congenital adrenal hyperplasia.

Adina F Turcu1, Richard J Auchus2.   

Abstract

Adrenal steroidogenesis is a dynamic process, reliant on de novo synthesis from cholesterol, under the stimulation of ACTH and other regulators. The syntheses of mineralocorticoids (primarily aldosterone), glucocorticoids (primarily cortisol), and adrenal androgens (primarily dehydroepiandrosterone and its sulfate) occur in separate adrenal cortical zones, each expressing specific enzymes. Congenital adrenal hyperplasia (CAH) encompasses a group of autosomal-recessive enzymatic defects in cortisol biosynthesis. 21-Hydroxylase (21OHD) deficiency accounts for more than 90% of CAH cases and, when milder or nonclassic forms are included, 21OHD is one of the most common genetic diseases.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  21-Hydroxylase; Adrenal insufficiency; Ambiguous genitalia; Androgen; Congenital adrenal hyperplasia; Disorder of sex development; Steroid hydroxylase; Steroidogenesis

Mesh:

Substances:

Year:  2015        PMID: 26038201      PMCID: PMC4506691          DOI: 10.1016/j.ecl.2015.02.002

Source DB:  PubMed          Journal:  Endocrinol Metab Clin North Am        ISSN: 0889-8529            Impact factor:   4.741


  136 in total

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