Clinical Phenotype of Musladin-Lueke Syndrome in 2 Beagles

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Abstract

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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Packer, R. A., Logan, M. A., Guo, L. T., Apte, S. S., Bader, H., O’Brien, D. P., … Shelton, G. D. (2017). Clinical Phenotype of Musladin-Lueke Syndrome in 2 Beagles. Journal of Veterinary Internal Medicine, 31(2), 532–538. https://doi.org/10.1111/jvim.14654

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