Evidence for a Continuum of Genetic, Phenotypic, and Biochemical Abnormalities in Children with Growth Hormone Insensitivity

Author:

David Alessia1,Hwa Vivian2,Metherell Louise A.1,Netchine Irène345,Camacho-Hübner Cecilia6,Clark Adrian J. L.1,Rosenfeld Ron G.2,Savage Martin O.1

Affiliation:

1. Department of Endocrinology (A.D., L.A.M., A.J.L.C., M.O.S.), William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, London EC1M 6BQ, United Kingdom;

2. Department of Pediatrics (V.H., R.G.R.), Oregon Health and Science University, Portland, Oregon 97239;

3. Hôpital Armand-Trousseau (I.N.), Explorations Fonctionnelles Endocriniennes, 75012 Paris, France;

4. Université Pierre et Marie Curie (I.N.), 75005 Paris, France;

5. Institut National de la Santé et de la Recherche Médicale (I.N.), Unité 938, Team 4, 75012 Paris, France;

6. Karolinska Institute (C.C.-H.), 171 65 Stockholm, Sweden

Publisher

The Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference184 articles.

1. Genetic pituitary dwarfism with high serum concentration of growth hormone—a new inborn error of metabolism?;Laron;Isr J Med Sci,1966

2. Laron syndrome (primary growth hormone resistance or insensitivity): the personal experience 1958–2003;Laron;J Clin Endocrinol Metab,2004

3. Defect of human growth hormone receptors in the liver of two patients with Laron-type dwarfism;Eshet;Isr J Med Sci,1984

4. Effect of acute administration of insulin-like growth factor I in patients with Laron-type dwarfism;Laron;Lancet,1988

5. Effects of the infusion of insulin-like growth factor I in a child with growth hormone insensitivity syndrome (Laron dwarfism);Walker;N Engl J Med,1991

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