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The insulin-like growth factors and growth disorders of childhood.

Abstract
Specific lesions of the growth hormone (GH)/insulin-like growth factor (IGF) axis have been identified in humans, each of which has distinctive auxologic and biochemical features. Measures of circulating IGF-I are useful in diagnosing growth disorders in childhood and in evaluating response to GH therapy. Recombinant human IGF-I is an effective treatment of severe primary IGF deficiency, which is typical of patients with GH receptor defects (Laron syndrome). Such treatment has been limited to a few severely affected patients. Future studies will provide new insight into IGF-I as treatment and into the nature of growth disorders that involve the IGF axis.
AuthorsPhilippe F Backeljauw, Steven D Chernausek
JournalEndocrinology and metabolism clinics of North America (Endocrinol Metab Clin North Am) Vol. 41 Issue 2 Pg. 265-82, v (Jun 2012) ISSN: 1558-4410 [Electronic] United States
PMID22682630 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2012 Elsevier Inc. All rights reserved.
Chemical References
  • Insulin-Like Growth Factor Binding Proteins
  • Intercellular Signaling Peptides and Proteins
  • Recombinant Proteins
  • Somatomedins
  • myotrophin
Topics
  • Child
  • Female
  • Growth Disorders (diagnosis, drug therapy, metabolism)
  • Humans
  • Insulin-Like Growth Factor Binding Proteins (blood, physiology)
  • Intercellular Signaling Peptides and Proteins (therapeutic use)
  • Laron Syndrome (drug therapy, metabolism)
  • Male
  • Recombinant Proteins (therapeutic use)
  • Somatomedins (deficiency, genetics, therapeutic use)
  • Treatment Outcome

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