Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://www.nature.com/articles/ncpendmet0481.pdf
Reference67 articles.
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3. White PC and Speiser PW (2000) Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev 21: 245–291
4. Hughes IA et al. (2006) Consensus statement on management of intersex disorders. Arch Dis Child 91: 554–563
5. Crouch NS and Creighton SM (2004) Minimal surgical intervention in the management of intersex conditions. J Pediatr Endocrinol Metab 17: 1591–1596
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2. The importance and implications of preconception genetic testing for accurate fetal risk estimation in 21-hydroxylase congenital adrenal hyperplasia (CAH);Gynecological Endocrinology;2018-07-25
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