| Literature DB >> 15761234 |
Patricia Park1, Pinchas Cohen.
Abstract
Growth hormone (GH) therapy has evolved rapidly over the past decade, and continuing research has established a clear role for therapeutic GH in a wide spectrum of disorders, including idiopathic GH deficiency (childhood- and adult-onset), Turner syndrome, Prader-Willi syndrome, small-for-gestational age children with failure of catch-up growth, AIDS-related catabolism, children with chronic renal failure, and idiopathic short stature. Although GH is used therapeutically in a wide variety of conditions, actual guidelines regarding the logistics of GH dosing continue to evolve, with data emerging regarding efficacy and safety. This review proposes a role for insulin-like growth factor I measurement in optimizing GH dosing. Copyright 2004 S. Karger AG, Basel.Entities:
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Year: 2004 PMID: 15761234 DOI: 10.1159/000080760
Source DB: PubMed Journal: Horm Res ISSN: 0301-0163