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The nature of fibrous dysplasia
Fibrous dysplasia has been regarded as a developmental skeletal disorder characterized by replacement of normal bone with benign cellular fibrous connective tissue. It has now become evident that fibrous dysplasia is a genetic disease caused by somatic activating mutation of the Gsα subunit of G pro...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779176/ https://www.ncbi.nlm.nih.gov/pubmed/19895712 http://dx.doi.org/10.1186/1746-160X-5-22 |
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author | Feller, Liviu Wood, Neil H Khammissa, Razia AG Lemmer, Johan Raubenheimer, Erich J |
author_facet | Feller, Liviu Wood, Neil H Khammissa, Razia AG Lemmer, Johan Raubenheimer, Erich J |
author_sort | Feller, Liviu |
collection | PubMed |
description | Fibrous dysplasia has been regarded as a developmental skeletal disorder characterized by replacement of normal bone with benign cellular fibrous connective tissue. It has now become evident that fibrous dysplasia is a genetic disease caused by somatic activating mutation of the Gsα subunit of G protein-coupled receptor resulting in upregulation of cAMP. This leads to defects in differentiation of osteoblasts with subsequent production of abnormal bone in an abundant fibrous stroma. In addition there is an increased production of IL-6 by mutated stromal fibrous dysplastic cells that induce osteoclastic bone resorption. |
format | Text |
id | pubmed-2779176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27791762009-11-19 The nature of fibrous dysplasia Feller, Liviu Wood, Neil H Khammissa, Razia AG Lemmer, Johan Raubenheimer, Erich J Head Face Med Review Fibrous dysplasia has been regarded as a developmental skeletal disorder characterized by replacement of normal bone with benign cellular fibrous connective tissue. It has now become evident that fibrous dysplasia is a genetic disease caused by somatic activating mutation of the Gsα subunit of G protein-coupled receptor resulting in upregulation of cAMP. This leads to defects in differentiation of osteoblasts with subsequent production of abnormal bone in an abundant fibrous stroma. In addition there is an increased production of IL-6 by mutated stromal fibrous dysplastic cells that induce osteoclastic bone resorption. BioMed Central 2009-11-09 /pmc/articles/PMC2779176/ /pubmed/19895712 http://dx.doi.org/10.1186/1746-160X-5-22 Text en Copyright ©2009 Feller et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Feller, Liviu Wood, Neil H Khammissa, Razia AG Lemmer, Johan Raubenheimer, Erich J The nature of fibrous dysplasia |
title | The nature of fibrous dysplasia |
title_full | The nature of fibrous dysplasia |
title_fullStr | The nature of fibrous dysplasia |
title_full_unstemmed | The nature of fibrous dysplasia |
title_short | The nature of fibrous dysplasia |
title_sort | nature of fibrous dysplasia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779176/ https://www.ncbi.nlm.nih.gov/pubmed/19895712 http://dx.doi.org/10.1186/1746-160X-5-22 |
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