Journal of the Bahrain Medical Society

Year 2014, Volume 25, Issue 2, Pages 108-111

http://doi.org/10.26715/jbms.25_2_11

Case Report

11-beta hydroxylase deficiency in children: the first case reported from Bahrain

Mansoor H. Rajab,* Abdul Raoof Almadhoob,** Hasan M. Isa ***

Author Affiliation

*Consultant Pediatric Endocrinologist, Salmaniya Medical Complex, Kingdom of Bahrain
**Consultant Pediatric Neonatologist, Salmaniya Medical Complex, Kingdom of Bahrain
***Consultant Pediatric Gastroenterologist, Salmaniya Medical Complex, Kingdom of Bahrain

Correspondence to: drmansoorrajab@hotmail.com


Abstract

Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder commonly caused by 21-hydroxylase deficiency. It accounts for 90-95% of cases. The second most common cause is 11β hydroxylase deficiency. We report on the first case of 11β hydroxylase deficiency in Bahrain with a review of the literature.

Keywords: 11β hydroxylase deficiency; congenital adrenal hyperplasia (CAH)