21-hydroxylase deficiency primary prevention

Congenital adrenal hyperplasia main page
Overview
Classification 21-hydroxylase deficiency
11β-hydroxylase deficiency
17 alpha-hydroxylase deficiency
3 beta-hydroxysteroid dehydrogenase deficiency
Cytochrome P450-oxidoreductase (POR) deficiency (ORD)
Lipoid congenital adrenal hyperplasia
Differential Diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Primary Prevention

• Doctors often recommend genetic counseling for parents who have congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Early diagnosis during pregnant peroid can minimize or even eliminate symptoms after birth.