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COL6A1 related muscular dystrophy in Landseer dogs: A canine model for Ullrich congenital muscular dystrophy
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AbstractBackgroundCollagen VI related myopathies are congenital diseases of variable phenotype. The severe phenotype is referred to as Ullrich congenital muscular dystrophy. In this study, we describe analoguos clinical signs and histopathological alterations in Landseer dogs.MaterialsWe collected clinical data from two affected dogs and investigated the neuromuscular changes in five dogs from two different litters with immunohistochemistry and immunofluorescence. All affected dogs were homozygous for the p.Glu97* nonsense variant in the COL6A1 gene encoding the alpha‐1 chain of collagen VI.ResultsMuscle biopsies revealed alterations similar to those in human patients with Ullrich congenital muscular dystrophy including the virtual absence of collagen VI in skeletal muscles.ConclusionsThe clinical and pathological characterization of the affected Landseer dogs enhances the value of this animal model for human Ullrich congenital muscular dystrophy.
Title: COL6A1 related muscular dystrophy in Landseer dogs: A canine model for Ullrich congenital muscular dystrophy
Description:
AbstractBackgroundCollagen VI related myopathies are congenital diseases of variable phenotype.
The severe phenotype is referred to as Ullrich congenital muscular dystrophy.
In this study, we describe analoguos clinical signs and histopathological alterations in Landseer dogs.
MaterialsWe collected clinical data from two affected dogs and investigated the neuromuscular changes in five dogs from two different litters with immunohistochemistry and immunofluorescence.
All affected dogs were homozygous for the p.
Glu97* nonsense variant in the COL6A1 gene encoding the alpha‐1 chain of collagen VI.
ResultsMuscle biopsies revealed alterations similar to those in human patients with Ullrich congenital muscular dystrophy including the virtual absence of collagen VI in skeletal muscles.
ConclusionsThe clinical and pathological characterization of the affected Landseer dogs enhances the value of this animal model for human Ullrich congenital muscular dystrophy.
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