Diagnosis, treatment and preventive measures in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in patients in adulthood
Н В Молашенко, А И Сазонова, Е. А. Трошина
Abstract
Н В Молашенко, А И Сазонова, Е. А. Трошина
Abstract
In the article there are presented main approaches to the diagnosis, treatment and follow-up of patients with classical and nonclassical forms of 21-hydroxylase deficiency. The techniques of diagnostic tests and parameters of hormonal indices for the assessment of the adequacy of replacement therapy with glucocorticoids and mineralocorticoids are considered.
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In the article there are presented main approaches to the diagnosis, treatment and follow-up of patients with classical and nonclassical forms of 21-hydroxylase deficiency. The techniques of diagnostic tests and parameters of hormonal indices for the assessment of the adequacy of replacement therapy with glucocorticoids and mineralocorticoids are considered.
Key concepts: Congenital adrenal hyperplasia, 21-Hydroxylase, Medicine, Pediatrics, Internal medicine, Endocrinology