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Article

Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Feb 2005

Motaghedi R, Betensky B P, Slowinska B, Cerame B, Cabrer M, New M I, Wilson R C

Abstract excerpt

11beta-Hydroxylase deficiency is a common form of congenital adrenal hyperplasia causing virilization of the female fetus and hypertension. DNA analysis of the gene (CYP11B1) encoding 11beta-hydroxylase has been reported previously to be effective in the prenatal diagnosis of one affected female fetus. In that case, prenatal treatment with dexamethasone resulted in normal female genitalia. We now report five new...

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Source

Identifiers

PMID: 15751602
DOI: 10.1515/jpem.2005.18.2.133

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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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Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency in a Tunisian family.Semantic proximity Read ↗

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Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiencySemantic proximity Read ↗

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