Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency

Author:

Costa-Barbosa Flávia A.,Tonetto-Fernandes Vânia F.,Carvalho Valdemir M.,Nakamura Odete H.,Moura Vivian,Bachega Tânia A. S. S.,Vieira José G. H.,Kater Claudio E.

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference40 articles.

1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocrine Reviews,2000

2. Congenital adrenal hyperplasia;Speiser;New England Journal of Medicine,2003

3. Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia;Moran;Journal of Clinical Endocrinology and Metabolism,2006

4. Extensive clinical experience: nonclassical 21-hydroxylase deficiency;New;Journal of Clinical Endocrinology and Metabolism,2006

5. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Forest;Human Reproduction Update,2004

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1. Plasma 21-deoxycortisone: a sensitive additive tool in 21-hydroxylase deficiency in newborns;European Journal of Endocrinology;2024-08

2. Serum 21-Deoxycortisol for Diagnosis of Nonclassic Congenital Adrenal Hyperplasia in Women With Androgen Excess;The Journal of Clinical Endocrinology & Metabolism;2023-06-26

3. Hypergonadism;Steroids in the Laboratory and Clinical Practice;2023

4. The uncommon forms of congenital adrenal hyperplasia;Current Opinion in Endocrinology, Diabetes & Obesity;2022-06

5. Acton-Prolongatum Stimulated Blood Steroid Profile in Apparently Healthy Asian Indian Women of Reproductive-Age Group;Indian Journal of Clinical Biochemistry;2022-04-30

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