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 …

Deficiency of the 21-hydroxylase enzyme is the most common form of congenital adrenal
hyperplasia (CAH), accounting for more than 95% of the cases. With the advent of newborn …

Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive diseases that may
cause cortisol insufficiency together with other hormonal alterations. The most common form …

Congenital adrenal hyperplasia (CAH) refers to a group of disorders that are associated with
defective adrenal steroidogenesis, the most common of which is 21-hydroxylase deficiency …

Background: Congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency
accounts for 95% of all CAH cases and is one the most common inborn metabolic disorders …

Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders of
steroidogenesis of the adrenal cortex, most commonly due to 21-hydroxylase deficiency …

Background. Our knowledge on long-term outcome in CAH remains incomplete. Methods. In
a prospective study (33 CAH patients, 33 age-matched controls), reproductive outcomes …

Congenital adrenal hyperplasia (CAH) describes a group of autosomal recessive disorders
where there is impairment of cortisol biosynthesis. CAH due to 21-hydroxylase deficiency …

Congenital adrenal hyperplasia (CAH) most commonly due to 21-hydroxylase deficiency is
the most common type of disorder of sex development. This review will focus on CAH …

The adolescent period is characterised by fundamental hormonal changes, which affect sex
steroid production, cortisol metabolism and insulin sensitivity. These physiological changes …