Growth hormone and its disorders
- PMID: 16397076
- PMCID: PMC2563724
- DOI: 10.1136/pgmj.2005.036087
Growth hormone and its disorders
Abstract
Growth hormone (GH) is synthesised and secreted by the somatotroph cells of the anterior lobe of the pituitary gland. Its actions involve multiple organs and systems, affecting postnatal longitudinal growth as well as protein, lipid, and carbohydrate metabolism. GH hypersecretion results in gigantism or acromegaly, a condition associated with significant morbidity and mortality, while GH deficiency results in growth retardation in children and the GH deficiency syndrome in adults. This article, aimed at non-paediatric physicians, examines the clinical features, diagnosis, and current concepts in the management of these conditions.
Conflict of interest statement
Conflicts of interest: none.
References
-
- de Vos A M, Ultsch M, Kossiakoff A A. Human growth hormone and extracellular domain of its receptor: crystal structure of the complex. Science 1992255306–312. - PubMed
-
- Cunningham B C, Ultsch M, de Vos A M.et al Dimerization of the extracellular domain of the human growth hormone receptor by a single hormone molecule. Science 1991254821–825. - PubMed
-
- Argetsinger L S, Carter‐Su C. Mechanism of signaling by growth hormone receptor. Physiol Rev 1996761089–1107. - PubMed
-
- Gluckman P D, Grumbach M M, Kaplan S L. The neuroendocrine regulation and function of growth hormone and prolactin in the mammalian fetus. Endocr Rev 19812363–395. - PubMed
-
- Le Roith D, Bondy C, Yakar S.et al The somatomedin hypothesis: 2001. Endocr Rev 20012253–74. - PubMed
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