Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta

Achondroplasia, Duchenne muscular dystrophy, and osteogenesis imperfecta are among the most frequent rare genetic disorders affecting the musculoskeletal system in children. Rare genetic disorders are severely disabling and can have substantial impacts on families, children, and on healthcare system...

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Autores principales: Dogba, Maman Joyce, Rauch, Frank, Douglas, Erin, Bedos, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332447/
https://www.ncbi.nlm.nih.gov/pubmed/25649344
http://dx.doi.org/10.1186/s12955-014-0151-y
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author Dogba, Maman Joyce
Rauch, Frank
Douglas, Erin
Bedos, Christophe
author_facet Dogba, Maman Joyce
Rauch, Frank
Douglas, Erin
Bedos, Christophe
author_sort Dogba, Maman Joyce
collection PubMed
description Achondroplasia, Duchenne muscular dystrophy, and osteogenesis imperfecta are among the most frequent rare genetic disorders affecting the musculoskeletal system in children. Rare genetic disorders are severely disabling and can have substantial impacts on families, children, and on healthcare systems. This literature review aims to classify, summarize and compare these non-medical impacts of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta.
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spelling pubmed-43324472015-02-19 Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta Dogba, Maman Joyce Rauch, Frank Douglas, Erin Bedos, Christophe Health Qual Life Outcomes Review Achondroplasia, Duchenne muscular dystrophy, and osteogenesis imperfecta are among the most frequent rare genetic disorders affecting the musculoskeletal system in children. Rare genetic disorders are severely disabling and can have substantial impacts on families, children, and on healthcare systems. This literature review aims to classify, summarize and compare these non-medical impacts of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta. BioMed Central 2014-10-25 /pmc/articles/PMC4332447/ /pubmed/25649344 http://dx.doi.org/10.1186/s12955-014-0151-y Text en © Dogba et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Dogba, Maman Joyce
Rauch, Frank
Douglas, Erin
Bedos, Christophe
Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta
title Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta
title_full Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta
title_fullStr Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta
title_full_unstemmed Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta
title_short Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta
title_sort impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, duchenne muscular dystrophy and osteogenesis imperfecta
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332447/
https://www.ncbi.nlm.nih.gov/pubmed/25649344
http://dx.doi.org/10.1186/s12955-014-0151-y
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