The Adrenal
- 1 October 2004
- journal article
- review article
- Published by S. Karger AG in Hormone Research in Paediatrics
- Vol. 62 (Suppl. 3) , 22-29
- https://doi.org/10.1159/000080495
Abstract
During the past 15 years, considerable progress has been made in our understanding of the genetic basis of adrenal development and function. More than 30 single gene disorders have now been identified that can affect the hypothalamic-pituitary-adrenal axis in humans (fig. 1, 2; table 1). This review highlights recent advances in the molecular pathology of: (1) adrenal hypoplasia, (2) adrenal destruction, (3) disorders of adrenal steroidogenesis, (4) adrenal steroid resistance and (5) activation of the adrenal axis/tumorigenesis. Characterizing the molecular basis and natural history of these conditions is providing fascinating insight into adrenal development and function and can help to focus treatment and counselling of patients appropriately. However, ongoing translation of research findings into clinical practice is needed if patient care is to be influenced significantly.Keywords
This publication has 52 references indexed in Scilit:
- Smith‐Lemli‐Opitz Syndrome and the DHCR7 GeneAnnals of Human Genetics, 2003
- Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune diseaseNature, 2003
- Compound Heterozygous Mutations in the Cholesterol Side-Chain Cleavage Enzyme Gene (CYP11A) Cause Congenital Adrenal Insufficiency in HumansJournal of Clinical Endocrinology & Metabolism, 2002
- Gene profiling of human fetal and adult adrenalsJournal of Endocrinology, 2001
- Dehydroepiandrosterone replacement for patients with adrenal insufficiencyThe Lancet, 2001
- Congenital Adrenal Hyperplasia due to 21-Hydroxylase DeficiencyEndocrine Reviews, 2000
- Longitudinal Hormonal and Pituitary Imaging Changes in Two Females with Combined Pituitary Hormone Deficiency due to Deletion of A301,G302 in the PROP1 GeneJournal of Clinical Endocrinology & Metabolism, 1999
- Adrenocorticotropin Insensitivity SyndromesEndocrine Reviews, 1998
- Hereditary Defect in Biosynthesis of Aldosterone: Aldosterone Synthase Deficiency 1964-1997Journal of Clinical Endocrinology & Metabolism, 1997
- X-linked adrenoleukodystrophy is a frequent cause of idiopathic Addison's disease in young adult male patientsJournal of Clinical Endocrinology & Metabolism, 1996