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

Bahrain Medical Society

Publication Date

2014-06-30

Country of Publication

Bahrain

No. of Pages

4

Main Subjects

Medicine

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