English RCCX Cited by user Maxim Masiutin on 24 Jan 2022 RCCX is a multiallelic copy number variation human DNA locus on chromosome 6p21.3. [edit] Structure The number of RCCX segments varies between one and four in a…
English Late onset congenital adrenal hyperplasia Cited by user Maxim Masiutin on 11 Nov 2020 The causes of LOCAH are the same as of classic CAH, and in the majority of the cases are the mutations in the CYP21A2 gene resulting in corresponding activity changes in…
English Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Cited by user Maxim Masiutin on 11 Nov 2020 Congenital adrenal hyperplasia due to 21-hydroxylase deficiency in all its forms, accounts for over 95% of diagnosed cases of congenital adrenal hyperplasia (CAH), and…