The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis

Author:

Ambroziak Urszula1,Kępczyńska-Nyk Anna1,Kuryłowicz Alina12,Małunowicz Ewa Maria3,Wójcicka Anna45,Miśkiewicz Piotr1,Macech Magdalena1

Affiliation:

1. Department of Internal Medicine and Endocrinology; Medical University of Warsaw; Warsaw Poland

2. Department of Human Epigenetics; Mossakowski Medical Research Centre; Polish Academy of Sciences; Warsaw Poland

3. Department of Biochemistry, Radioimmunology and Experimental Medicine; Children's Memorial Health Institute; Warsaw Poland

4. Genomic Medicine; Medical University of Warsaw; Warsaw Poland

5. Laboratory of Human Cancer Genetics; Centre of New Technologies, CENT; University of Warsaw; Warsaw Poland

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference31 articles.

1. Diagnosis of hyperandrogenism: clinical criteria;Yildiz;Best Practice & Research. Clinical Endocrinology & Metabolism,2006

2. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency - management in adults;Ambroziak;Endokrynologia Polska,2010

3. Polycystic ovary syndrome;Ehrmann;New England Journal of Medicine,2005

4. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline;Speiser;Journal of Clinical Endocrinology and Metabolism,2010

5. A prospective study of the prevalence of nonclassical congenital adrenal hyperplasia among women presenting with hyperandrogenic symptoms and signs;Escobar-Morreale;Journal of Clinical Endocrinology and Metabolism,2008

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