Congenital adrenal hyperplasia
Congenital adrenal cortical hyperplasia (CAH) is a group of diseases caused by congenital defects of one or more enzymes in the adrenal cortical hormone biosynthesis enzyme system, which changes the levels of hormones such as cortisol. It is often autosomal recessive. Clinically, 21-hydroxylase deficiency is the most common, accounting for more than 90%, with an incidence of about 1/4500 newborns, of which about 75% are salt-losing type, followed by 11β-hydroxylase deficiency, accounting for about 5% to 8%, with an incidence of about 1/5000 to 7000 newborns. Other types are rare.
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Site of disease:
Adrenal glands -
Infectious :
Not contagious -
Frequent population:
More common in children -
Related symptoms:
Hypertestosteronemia Bilateral adrenal hyperplasia Post-pubertal azoospermia Excessive secretion of mineralocorticoids 21-hydroxylase deficiency -
Concurrent disease:
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Hydrocortisone tablets
Indication: It is mainly used for replacement therapy of adrenal insufficiency and congenital adrenal hyperplasia.
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Indication: It is mainly used for replacement therapy of adrenal insufficiency and congenital adrenal hyperplasia.
Hydrocortisone tablets
Indication: It is mainly used for replacement therapy of adrenal insufficiency and congenital adrenal hyperplasia.
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Hydrocortisone tablets
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