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Congenital adrenal hyperplasia due to 21‐hydroxylase deficiency

1 Apr 2010

Abstract excerpt

21-Hydroxylase deficiency is the most common cause of congenital adrenal hyperplasia (CAH), an inherited disorder of steroidogenesis. In its severe form, CAH causes genital ambiguity in females. Molecular genetic analysis of fetal DNA obtained by amniocentesis or chorionic villus sampling is used to diagnose steroid 21-OHD deficiency in utero. Large ongoing studies show that appropriate prenatal treatment of...

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PMID: 20392211
DOI: 10.1111/j.1749-6632.2009.05225.x

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