11β-hydroxylase deficiency classification

Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]

Overview

Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency may be classified according to the clinical presentation into 2 subtypes: the classic form of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency and the non-classic form of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Classification

There are two types of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency, classic form of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency and the non-classic form of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.