Acromegaly (cont.)Medical Author:
Hasnain M Khandwala, MD, FRCPC
Medical Editor:
Arthur B Chausmer, MD, PhD, FACP, FACE, FACN, CNS
Medical Editor:
Francisco Talavera, PharmD, PhD
Medical Editor:
George T Griffing, MD
IN THIS ARTICLE
Authors and EditorsAuthor: Hasnain M Khandwala, MD, FRCPC, Assistant Professor, Department of Medicine, Division of Endocrinology, University of Saskatchewan, Canada.Editors: Arthur B Chausmer, MD, PhD, FACP, FACE, FACN, CNS, Affiliate Research Professor, Bioinformatics and Computational Biology Program, School of Computational Sciences; Principal, C/A Informatics, LLC; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; George T Griffing, MD, Director, Division of General Internal Medicine, Professor, Department of Internal Medicine, St Louis University. Last Editorial Review: 11/16/2009 |
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Acromegaly »
Increased and unregulated growth hormone (GH) production, usually caused by a GH-secreting pituitary tumor (somatotroph tumor), characterizes acromegaly.
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