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Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles

R.A. Packer et al · Oxford University Press · 2017

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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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APA 7

al, R. P. E. (2017). Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles. https://doi.org/10.1111/jvim.14654

MLA

al, R.A. Packer et. "Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles." 2017. https://doi.org/10.1111/jvim.14654.

Chicago

al, R.A. Packer et. 2017. "Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles.". https://doi.org/10.1111/jvim.14654.

Harvard

al, R. P. E. 2017, Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles, Oxford University Press, available at: https://doi.org/10.1111/jvim.14654 [Accessed 5 Aug. 2026].

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Title
Clinical Phenotype of Musladin‐Lueke Syndrome in 2 Beagles
Author / contributors
R.A. Packer et al
Publisher
Oxford University Press
Publication year
2017
ISSN
0891-6640
ISSN
0891-6640
Language
English

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