Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report

Objective. To describe a biochemical growth hormone (GH) deficiency and to evaluate therapeutic result in a six-year-old male with Becker muscular dystrophy (BMD). Methods. GH peak was evaluated after response to arginine and insulin. Bone age was evaluated according to Greulich and Pyle method. Re...

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Main Authors: Valeria Calcaterra, Annachiara Malvezzi, Rossana Toglia, Angela Berardinelli, Elena Bozzola, Mauro Bozzola, Daniela Larizza
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Case Reports in Endocrinology
Online Access:http://dx.doi.org/10.1155/2013/684249
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author Valeria Calcaterra
Annachiara Malvezzi
Rossana Toglia
Angela Berardinelli
Elena Bozzola
Mauro Bozzola
Daniela Larizza
author_facet Valeria Calcaterra
Annachiara Malvezzi
Rossana Toglia
Angela Berardinelli
Elena Bozzola
Mauro Bozzola
Daniela Larizza
author_sort Valeria Calcaterra
collection DOAJ
description Objective. To describe a biochemical growth hormone (GH) deficiency and to evaluate therapeutic result in a six-year-old male with Becker muscular dystrophy (BMD). Methods. GH peak was evaluated after response to arginine and insulin. Bone age was evaluated according to Greulich and Pyle method. Results. The GH-supplementary therapy was very effective in terms of growth gain. Conclusion. The possibility of a growth hormone deficiency and treatment with GH in patients with BMD cannot be excluded, especially considering the good therapeutic response.
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institution Kabale University
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publishDate 2013-01-01
publisher Wiley
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series Case Reports in Endocrinology
spelling doaj-art-265b973a0e6f4dfdbdaba65caa0d2e0f2025-02-03T01:29:00ZengWileyCase Reports in Endocrinology2090-65012090-651X2013-01-01201310.1155/2013/684249684249Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case ReportValeria Calcaterra0Annachiara Malvezzi1Rossana Toglia2Angela Berardinelli3Elena Bozzola4Mauro Bozzola5Daniela Larizza6Department of Internal Medicine, University of Pavia, 27100 Pavia, ItalyDepartment of Pediatrics, IRCCS Policlinico S. Matteo Foundation, 27100 Pavia, ItalyDepartment of Pediatrics, IRCCS Policlinico S. Matteo Foundation, 27100 Pavia, ItalyIRCCS C. Mondino Foundation and University of Pavia, 27100 Pavia, ItalyPediatric and Infectious Disease Unit, Department of Pediatrics, Bambino Gesù Children’s Hospital, 00165 Rome, ItalyDepartment of Internal Medicine, University of Pavia, 27100 Pavia, ItalyDepartment of Internal Medicine, University of Pavia, 27100 Pavia, ItalyObjective. To describe a biochemical growth hormone (GH) deficiency and to evaluate therapeutic result in a six-year-old male with Becker muscular dystrophy (BMD). Methods. GH peak was evaluated after response to arginine and insulin. Bone age was evaluated according to Greulich and Pyle method. Results. The GH-supplementary therapy was very effective in terms of growth gain. Conclusion. The possibility of a growth hormone deficiency and treatment with GH in patients with BMD cannot be excluded, especially considering the good therapeutic response.http://dx.doi.org/10.1155/2013/684249
spellingShingle Valeria Calcaterra
Annachiara Malvezzi
Rossana Toglia
Angela Berardinelli
Elena Bozzola
Mauro Bozzola
Daniela Larizza
Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report
Case Reports in Endocrinology
title Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report
title_full Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report
title_fullStr Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report
title_full_unstemmed Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report
title_short Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report
title_sort growth hormone deficiency in a patient with becker muscular dystrophy a pediatric case report
url http://dx.doi.org/10.1155/2013/684249
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