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Article

Congenital Adrenal Hyperplasia.

Journal of pediatric and adolescent gynecology - 1 Oct 2017

Witchel Selma Feldman

Abstract excerpt

The congenital adrenal hyperplasias comprise a family of autosomal recessive disorders that disrupt adrenal steroidogenesis. The most common form is due to 21-hydroxylase deficiency associated with mutations in the 21-hydroxylase gene, which is located at chromosome 6p21. The clinical features associated with each disorder of adrenal steroidogenesis represent a clinical spectrum that reflect the consequences of...

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Identifiers

PMID: 28450075
DOI: 10.1016/j.jpag.2017.04.001
PMCID: PMC5624825

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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