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Growth hormone and its disorders
Author(s) -
John Ayuk,
Michael C. Sheppard
Publication year - 2006
Publication title -
postgraduate medical journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.568
H-Index - 99
eISSN - 1469-0756
pISSN - 0032-5473
DOI - 10.1136/pgmj.2005.036087
Subject(s) - gigantism , acromegaly , medicine , somatotropic cell , growth hormone , growth hormone deficiency , endocrinology , pituitary gland , pituitary disorder , hormone , growth retardation , pediatrics , bioinformatics , physiology , pregnancy , biology , genetics
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.

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