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Classic congenital adrenal hyperplasia
- ... 21 hydroxylase deficiency CYP21 deficiency Genetic Testing Registry: Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Genetic Testing Registry: ...
- ... dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2002 Jun;87(6): ...
- ... dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2002 Jun;87(6): ...
- ... Hypertension is not a feature of the non-classic form of CAH due to 11-beta-hydroxylase deficiency. CAH due to 11-beta-hydroxylase deficiency accounts for 5 to 8 percent of all cases of congenital adrenal hyperplasia. It is estimated that CAH due to 11- ...
- ... mutations associated with nonclassic and three mutations causing classic ... hyperplasia: 11beta-hydroxylase deficiency. Semin Reprod Med. 2002 Aug; ...
- ... 2 cytochrome P450, subfamily XXIA (steroid 21-hydroxylase, congenital adrenal hyperplasia), polypeptide 2 Cytosteroid 21-Monooxygenase P450c21B steroid 21- ...