Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders affecting
cortisol biosynthesis. Reduced activity of an enzyme required for cortisol production leads to …

Congenital adrenal hyperplasia (CAH) due to 21α-hydroxylase deficiency (21OHD) or 11β-
hydroxylase deficiency (11OHD) are congenital conditions with affected adrenal …

Many patients with congenital adrenal hyperplasia (CAH) refrain from seeking pregnancy,
suffer from infertility or worry about pregnancy complications, mainly due to genitalia …

Pediatric adrenocortical hyperplasias are rare; they usually present with Cushing syndrome
(CS); of them, isolated micronodular adrenal disease and its variant, primary pigmented …

Hydroxylase deficiency (21OHD) is the most common cause of congenital adrenal
hyperplasia. Increased production of adrenal-derived androgens and progesterone in …

Congenital adrenal hyperplasia (CAH) consists of a group of autosomal recessive disorders
resulting from enzymatic defects in steroidogenesis. More than 95% of CAH cases result …

Objective To compare clinical outcomes of 3 treatment regimens—glucocorticoids (GCs),
oral contraceptives (OCs), or a combination of both—administered to adolescents and …

Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder affecting cortisol
and aldosterone biosynthesis, which can lead to virilization in fetuses with a 46, XX …

Background: Menstrual irregularities may predict over adverse consequences in polycystic
ovary syndrome (PCOS). Objective: To observe the relation of variants of menstrual cycles …

Discussion: The principal aim of the management at adolescent age is to block
hyperandrogenism and to prevent or manage the complications of classic form and its …