Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OHD) in adult males: Clinical presentation, hormone function and the detection of adrenal and testicular adrenal rest tumors (TARTs)

Author:

San Martín Patricia,Eugenio Russmann María Laura,Mendeluk Gabriela,Fierro María Fabiana,Marino Roxana,Pardes Ester

Publisher

Elsevier BV

Subject

Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism

Reference43 articles.

1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency in South Africa;Speiser;Endocr Rev,2000

2. Congenital adrenal hyperplasia;Azziz;J Pediatr Adolesc Gynecol,2011

3. Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patients;Arlt;J Clin Endocrinol Metab,2010

4. Congenital adrenal hyperplasia;White;N Engl J Med,2003

5. Clinical outcome, hormonal status, gonadotrope axis, and testicular function in 219 adult men born with classic 21-hydroxylase deficiency. A French national survey;Bouvattier;J Clin Endocrinol Metab,2015

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