Rare forms of genetic paediatric adrenal insufficiency: Excluding congenital adrenal hyperplasia.
Ontology highlight
ABSTRACT: Adrenal insufficiency (AI) is a severe endocrine disorder characterized by insufficient glucocorticoid (GC) and/or mineralocorticoid (MC) secretion by the adrenal glands, due to impaired adrenal function (primary adrenal insufficiency, PAI) or to insufficient adrenal stimulation by pituitary ACTH (secondary adrenal insufficiency, SAI) or tertiary adrenal insufficiency due to hypothalamic dysfunction. In this review, we describe rare genetic causes of PAI with isolated GC or combined GC and MC deficiencies and we also describe rare syndromes of isolated MC deficiency. In children, the most frequent cause of PAI is congenital adrenal hyperplasia (CAH), a group of adrenal disorders related to steroidogenic enzyme deficiencies, which will not be included in this review. Less frequently, severa
SUBMITTER: Hasenmajer V
PROVIDER: S-EPMC10023752 | biostudies-literature | 2023 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA