Molecular Analysis of CYP21A2 Gene Mutations among Congenital Adrenal Hyperplasia Patients in Iraq

A category of autosomal recessive illnesses known as congenital adrenal hyperplasia. 21-hydroxylase insufficiency is the most common. Iraq has yet to report on the analysis of CYP21A2 gene mutations. The goal of this study is to look at the range and frequency of CYP21A2 mutations in Iraqi CAH patients. From September 2014 to June 2015,…
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August 12, 2021 0