Full 2L QBank
Pediatrics Genetic and genetic disorders 1681be1d

Most common enzyme deficiency in congenital adrenal hyperplasia is

A
3 beta hydroxylase
B
11 beta hydroxylase
C
17 hydroxylase
D
21 alfa hydroxylase
High-Yield Explanation
congenital adrenal hyperplasia is a group of autosomal recessive defects in steroid synthesis characterised by deficiency of adrenocoical hormones The commonest form of congenital adrenal hyperplasia accounting for about 90% of cases is due to deficiency of 21-alpha hydroxylase It is associated with diminished synthesis of coisol and aldosterone Reference: Ghai TB of pediatrics 8th edition pg 526

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