Cardiovascular and Metabolic Outcomes in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis

Author:

Tamhane Shrikant123,Rodriguez-Gutierrez Rene34,Iqbal Anoop Mohamed5,Prokop Larry J1,Bancos Irina2,Speiser Phyllis W6,Murad Mohammad Hassan1ORCID

Affiliation:

1. Evidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota

2. Division of Endocrinology, Mayo Clinic, Rochester, Minnesota

3. Knowledge and Evaluation Research Unit, Mayo Clinic, Rochester, Minnesota

4. Division of Endocrinology, Hospital Universitario “Dr. José E. Gonzalez,” Universidad Autonoma de Nuevo León, Monterrey, México

5. Department of Pediatric Endocrinology, Division of Pediatrics and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota

6. Division of Pediatric Endocrinology, Cohen Children’s Medical Center and Zucker Hofstra Northwell School of Medicine, Lake Success, New York

Funder

Endocrine Society

Publisher

The Endocrine Society

Subject

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

Reference42 articles.

1. Genetics of congenital adrenal hyperplasia;Krone;Best Pract Res Clin Endocrinol Metab,2009

2. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline;Speiser;J Clin Endocrinol Metab,2010

3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: newborn screening and its relationship to the diagnosis and treatment of the disorder;Pang;Screening,1993

4. Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia;Therrell;Pediatrics,1998

5. Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasia;Ferenczi;J Clin Endocrinol Metab,1999

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