Pegvisomant for the Treatment of gsp-Mediated Growth Hormone Excess in Patients with McCune-Albright Syndrome

Author:

Akintoye Sunday O.1,Kelly Marilyn H.1,Brillante Beth1,Cherman Natasha1,Turner Sarah1,Butman John A.2,Robey Pamela G.1,Collins Michael T.1

Affiliation:

1. Craniofacial and Skeletal Diseases Branch (S.O.A., M.H.K., B.B., N.C., P.G.R., M.T.C., S.T.), Bethesda, Maryland 20892

2. Diagnostic Radiology Department (J.A.B.), Clinical Center, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference24 articles.

1. Osteitis fibrosa cystica: the case of a nine-year-old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism;McCune;Am J Dis Child,1936

2. Syndrome characterized by osteitis fibrosa disseminata, areas, of pigmentation, and endocrine dysfunction, with precocious puberty in females: report of 5 cases;Albright;N Engl J Med,1937

3. Collins MT 2004 McCune-Albright syndrome. Orphanet Online Database of Rare Diseases (http://www.orpha.net), INSERM SCII; Paris

4. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome;Weinstein;N Engl J Med,1991

5. Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome;Schwindinger;Proc Natl Acad Sci USA,1992

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