CONGENITAL ADRENAL HYPERPLASIA

Author:

Pang Songya

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference119 articles.

1. Allen DB, Hoffman GL, Mahy SL, et al: Improved precision of newborn screening for 21-hydroxylase deficiency congenital adrenal hyperplasia (21-OH CAH) using weight-adjusted criteria for 17-hydroxyprogesterone (17-OHP) levels. In Programs and Abstracts of the Pediatric Research, APS-SPR Annual Meeting, 1995, 37:P84A

2. Clinical review 56: Nonclassic adrenal hyperplasia. Current concepts;Azziz;J Clin Endocrinol Metab,1994

3. Abnormalities of 21-hydroxylase gene ratio and adrenal steroidogenesis in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to acute adrenal stimulation;Azziz;J Clin Endocrinol Metab,1991

4. The adrenogenital syndrome with deficiency of 3β-hydroxysteroid dehydrogenase;Bongiovanni;J Clin Invest,1962

5. The pathophysiology and genetics of congenital lipoid adrenal hyperplasia;Bose;N Engl J Med,1996

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