Congenital adrenal hyperplasia (First of two parts) Journal Article


Authors: White, P. C.; New, M. I.; Dupont, B.
Article Title: Congenital adrenal hyperplasia (First of two parts)
Abstract: (First of Two Parts) CONGENITAL adrenal hyperplasia results from an inherited defect in any of the five enzymatic steps required to synthesize Cortisol from cholesterol. A defect in a particular step may be manifested clinically, not only because cortisol and other steroid hormones are not synthesized effectively but also because precursor steroids proximal to the blocked step may accumulate and be shunted into other metabolic pathways, particularly that of androgen biosynthesis. For example, in one of the earliest reports (in 1865) of a case of congenital adrenal hyperplasia, de Crecchio described a person who was considered to be a female... © 1987, Massachusetts Medical Society. All rights reserved.
Keywords: review; diagnosis; endocrine system; etiology; human; priority journal; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; congenital adrenal hyperplasia; congenital disorder; adrenal hyperplasia, congenital; hydroxyprogesterone
Journal Title: New England Journal of Medicine
Volume: 316
Issue: 24
ISSN: 0028-4793
Publisher: Massachusetts Medical Society  
Date Published: 1987-06-11
Start Page: 1519
End Page: 1524
Language: English
DOI: 10.1056/nejm198706113162406
PUBMED: 3295543
PROVIDER: scopus
DOI/URL:
Notes: Review -- Export Date: 5 February 2021 -- Source: Scopus
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  1. Bo Dupont
    264 Dupont