儿童11- β羟化酶缺乏症:巴林报告的第一例

Journal of the Bahrain Medical Society = Majallat Jam'iyat al-Atibba' al-Bahrayniyah Pub Date : 2022-01-01 DOI:10.26715/jbms.25_2_11

M. Rajab, A. Almadhoob, H. Isa

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引用次数: 0

摘要

先天性肾上腺增生症(CAH)是一种常染色体隐性遗传病，通常由21-羟化酶缺乏引起。它占90-95%的病例。第二个最常见的原因是11β羟化酶缺乏。我们报告第一例11β羟化酶缺乏症在巴林与文献回顾。

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

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.

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Journal of the Bahrain Medical Society = Majallat Jam'iyat al-Atibba' al-Bahrayniyah

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