Non-classic congenital adrenal hyperplasia (NCAH) is a relatively common disorder
regardless of ethnicity, but most cases are never diagnosed, especially in males. A baseline …

This review provides the reader with current insights on testicular adrenal rest tumors
(TARTs), a complication in male patients with congenital adrenal hyperplasia (CAH). In …

Congenital adrenal hyperplasia (CAH) caused by 21‐hydroxylase deficiency accounts for
95% of all CAH cases and is one of the most common inborn metabolic conditions. The …

Nonclassic congenital adrenal hyperplasia (NCAH) is one of the most frequent autosomal
recessive disorders in man with a prevalence ranging from 0.1% in Caucasians up to a few …

Purpose 3β-hydroxysteroid dehydrogenase type 2 deficiency (3βHSD2D) is a very rare
variant of congenital adrenal hyperplasia (CAH) causing less than 0.5% of all CAH. The aim …

Objectives To evaluate the risks of depression and all-cause mortality, healthcare utilisation
costs and treatment adherence in congenital adrenal hyperplasia (CAH) in the United …

Adrenal diseases—including disorders such as Cushing's syndrome, Addison's disease,
pheochromocytoma, primary hyperaldosteronism and congenital adrenal hyperplasia—are …

Abstract Background Congenital Adrenal Hyperplasia (CAH) is an endocrine disorder
characterized by enzymatic deficiency in adrenal steroidogenesis, leading to adrenal …

Abstract Treatment of classic congenital adrenal hyperplasia (CAH) is directed at replacing
deficient hormones and reducing androgen excess. However, even in the era of early …

Background Testicular adrenal rest tumors (TARTs) are benign neoplasms affecting patients
with congenital adrenal hyperplasia (CAH). The prevalence of TART in adult patients with …