Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Author:

Merke Deborah P.1

Affiliation:

1. National Institutes of Health Clinical Center and Reproductive Biology and Medicine Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-1932

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference59 articles.

1. Congenital adrenal hyperplasia.;Merke;Lancet,2005

2. Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population.;Jaaskelainen;J Clin Endocrinol Metab,1997

3. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany.;Krone;J Clin Endocrinol Metab,2000

4. Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.;Speiser;J Clin Invest,1992

5. Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation.;Wedell;J Clin Endocrinol Metab,1994

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