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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...

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Autores principales: Packer, R.A., Logan, M.A., Guo, L.T., Apte, S.S., Bader, H., O'Brien, D.P., Johnson, G., Shelton, G.D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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