11β hydroxylase deficiency in children : the first case reported from Bahrain
Joint Authors
Isa, Hasan M.
Rajab, Mansur H.
al-Madhub, Abd al-Rauf
Source
Journal of the Bahrain Medical Society
Issue
Vol. 25, Issue 2 (30 Jun. 2014), pp.108-111, 4 p.
Publisher
Publication Date
2014-06-30
Country of Publication
Bahrain
No. of Pages
4
Main Subjects
Topics
Abstract EN
Congenital adrenal hyperplasia(CAH) is an autosomal recessive disorder commonly caused by21-hydroxylase deficiency.
It accounts for 90-95% of cases.
The second most common cause is lip hydroxylase deficiency.
We rejx)rt on the الآلة case of lip hydroxylase deficiency in Bahrain with a review of the literature.
American Psychological Association (APA)
Rajab, Mansur H.& al-Madhub, Abd al-Rauf& Isa, Hasan M.. 2014. 11β hydroxylase deficiency in children : the first case reported from Bahrain. Journal of the Bahrain Medical Society،Vol. 25, no. 2, pp.108-111.
https://search.emarefa.net/detail/BIM-400374
Modern Language Association (MLA)
Rajab, Mansur H.…[et al.]. 11β hydroxylase deficiency in children : the first case reported from Bahrain. Journal of the Bahrain Medical Society Vol. 25, no. 2 (2014), pp.108-111.
https://search.emarefa.net/detail/BIM-400374
American Medical Association (AMA)
Rajab, Mansur H.& al-Madhub, Abd al-Rauf& Isa, Hasan M.. 11β hydroxylase deficiency in children : the first case reported from Bahrain. Journal of the Bahrain Medical Society. 2014. Vol. 25, no. 2, pp.108-111.
https://search.emarefa.net/detail/BIM-400374
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 109-110
Record ID
BIM-400374