Congenital adrenal hyperplasia (CAH) describes a group of autosomal recessive disorders
where there is impairment of cortisol biosynthesis. CAH due to 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 disorders affecting adrenal steroid
synthesis. The most common form, 21-hydroxylase deficiency, leads to decreased …

Congenital adrenal hyperplasia (CAH) is a genetic disorder caused by defective
steroidogenesis that results in glucocorticoid deficiency; the most common underlying …

Congenital adrenal hyperplasia (CAH) describes a family of disorders that comes from
enzymatic deficiencies in cortisol production, with 21-hydroxylase deficiency causing∼ 90 …

Congenital adrenal hyperplasia is a group of autosomal recessive disorders caused by
enzyme deficiency which leads to defects in biosynthesis of steroid precursors. Most …

Classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency leads to
glucocorticoid and mineralocorticoid deficiency. Management should be viewed as a …

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

Background: Clinical management of patients with congenital adrenal hyperplasia (CAH)
involves treating hormonal deficiencies, addressing issues related to genital ambiguity …

Congenital adrenal hyperplasia (CAH) owing to 21-hydroxylase deficiency is a common
disorder, and is characterised by a defect in cortisol biosynthesis with or without a defect in …