AI Article Synopsis

  • The collage VI-related muscular dystrophies in humans vary in severity from conditions like Ullrich congenital muscular dystrophy to milder forms such as Bethlem myopathy, characterized by muscle weakness and joint issues.
  • These conditions impact both muscle and connective tissue, leading to symptoms like respiratory failure, joint hyperlaxity, and contractures.
  • Researchers have identified two specific COL6A3 mutations in Labrador Retrievers that cause similar congenital myopathies, showcasing parallels between the diseases in dogs and humans.

Article Abstract

The collagen VI-related muscular dystrophies in people include a broad spectrum of diseases ranging from the severe Ullrich congenital muscular dystrophy to the mild Bethlem myopathy. Clinical features are attributable to both muscle and connective tissue and include progressive muscle weakness and respiratory failure, hyperlaxity of distal joints, and progressive contracture of large joints. Here we describe two different COL6A3 pathogenic variants in Labrador Retriever dogs that result in autosomal recessive or autosomal dominant congenital myopathies with hyperlaxity of distal joints and joint contracture, similar to the condition in people.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292757PMC
http://dx.doi.org/10.1016/j.nmd.2020.03.005DOI Listing

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