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Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles
Musladin‐Lueke syndrome (MLS), previously termed Chinese Beagle syndrome, is an autosomal‐recessive connective tissue disorder characterized by extensive fibrosis of the skin and joints that was first identified in Beagles in the 1970s. Recent research identified a founder mutation (c.660C>T; p.R...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354057/ https://www.ncbi.nlm.nih.gov/pubmed/28158899 http://dx.doi.org/10.1111/jvim.14654 |
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author | Packer, R.A. Logan, M.A. Guo, L.T. Apte, S.S. Bader, H. O'Brien, D.P. Johnson, G. Shelton, G.D. |
author_facet | Packer, R.A. Logan, M.A. Guo, L.T. Apte, S.S. Bader, H. O'Brien, D.P. Johnson, G. Shelton, G.D. |
author_sort | Packer, R.A. |
collection | PubMed |
description | Musladin‐Lueke syndrome (MLS), previously termed Chinese Beagle syndrome, is an autosomal‐recessive connective tissue disorder characterized by extensive fibrosis of the skin and joints that was first identified in Beagles in the 1970s. Recent research identified a founder mutation (c.660C>T; p.R221C) in the ADAMTSL2 gene in Beagles with MLS. Here, we report the detailed clinical phenotype and laboratory findings in 2 Beagles affected with MLS. We discuss these findings in relation to the human disorder geleophysic dysplasia (GD), which also arises from recessive ADAMTSL2 mutations, and recent findings in Adamtsl2‐deficient mice. |
format | Online Article Text |
id | pubmed-5354057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53540572017-03-22 Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles Packer, R.A. Logan, M.A. Guo, L.T. Apte, S.S. Bader, H. O'Brien, D.P. Johnson, G. Shelton, G.D. J Vet Intern Med SMALL ANIMAL Musladin‐Lueke syndrome (MLS), previously termed Chinese Beagle syndrome, is an autosomal‐recessive connective tissue disorder characterized by extensive fibrosis of the skin and joints that was first identified in Beagles in the 1970s. Recent research identified a founder mutation (c.660C>T; p.R221C) in the ADAMTSL2 gene in Beagles with MLS. Here, we report the detailed clinical phenotype and laboratory findings in 2 Beagles affected with MLS. We discuss these findings in relation to the human disorder geleophysic dysplasia (GD), which also arises from recessive ADAMTSL2 mutations, and recent findings in Adamtsl2‐deficient mice. John Wiley and Sons Inc. 2017-02-03 2017 /pmc/articles/PMC5354057/ /pubmed/28158899 http://dx.doi.org/10.1111/jvim.14654 Text en Copyright © 2017 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | SMALL ANIMAL Packer, R.A. Logan, M.A. Guo, L.T. Apte, S.S. Bader, H. O'Brien, D.P. Johnson, G. Shelton, G.D. Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles |
title | Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles |
title_full | Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles |
title_fullStr | Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles |
title_full_unstemmed | Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles |
title_short | Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles |
title_sort | clinical phenotype of musladin‐lueke syndrome in 2 beagles |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354057/ https://www.ncbi.nlm.nih.gov/pubmed/28158899 http://dx.doi.org/10.1111/jvim.14654 |
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