Muscular Dystrophy, Ullrich Type
Breed: Landseer/ European Continental Type
Generic Phene Data
Breeds
Relevance Rating: There is some evidence or research available in this breed
General
Disease Name
Muscular Dystrophy, Ullrich Type
OMIA
1967
Gene Name
COL6A1
Mutation
c.289C>T
Test Type
Genetic Disease/Disorder
Details
Muscular dystrophy refers to a group of more than thirty genetic conditions, causing a breakdown in the muscles involved with movement. This skeletal muscle disease is characterized by a progressive degeneration, leading to loss of muscle function and a weakness. Symptoms include: muscle stiffness, gait issues, muscle weakening, difficulty swallowing, progressive weakness, muscle atrophy and enlargement, difficulty swallowing - sometimes caused by a thickening tongue, loss of muscle mass, tremors, deformity of the limbs. Age of onset can be present from birth or very early in life, progressing with age. This condition usually affects males, though female cases have been documented and are often misdiagnosed. This progressive disease is normally fatal, or leads to euthanasia.
Details 2
Muscular dystrophy refers to a group of more than thirty genetic conditions, causing a breakdown in the muscles involved with movement. This skeletal muscle disease is characterized by a progressive degeneration caused by fibrosis leading to loss of muscle function and a weakness. Symptoms include: muscle stiffness, gait issues, muscle weakening, difficulty swallowing, progressive weakness, plantigrade stance, muscle atrophy and enlargement, difficulty swallowing, loss of muscle mass, tremors, deformity of the limbs. Age of onset can be present from birth or very early in life, progressing with age. This condition usually affects males, though female cases have been documented and are often misdiagnosed. This progressive disease is normally fatal, or leads to euthanasia.
Published
Steffen, F., Bilzer, T., Brands, J., Golini, L., Jagannathan, V., Wiedmer, M., Drögemüller, M., Drögemüller, C., Leeb, T. : A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy. G3 (Bethesda) 5:2611-7, 2015. Pubmed reference: 26438297. DOI: 10.1534/g3.115.021923.
Published 2
Marioni-Henry, K., Haworth, P., Scott, H., Witte, P., Guo, L.T., Shelton, G.D. : Sarcolemmal specific collagen VI deficient myopathy in a Labrador Retriever. J Vet Intern Med 28:243-9, 2013. Pubmed reference: 24147807. DOI: 10.1111/jvim.12224.
Body/System/Process
Muscular
OMIA Url
Inheritance
AR
Breed Specific Info
Researched Breeds
Landseer
HSP Test-Specific Data
Genomia s.r.o
GTP
GTP Name
Genomia s.r.o
Breed
OMIA
GTP Disease Synonym
Muscular dystrophy Landseer Ullrich type
Gene Name
COL6A1
Mutation
c.289G>T
Mutation Comment
g.39303964G>T
Nature of test
mutation test
FCI Number
226
GTP Breed
Landseer/ European continental type
Wisdom Panel - Kinship
GTP
GTP Name
Wisdom Panel - Kinship
Breed
OMIA
Gene Name
COL6A1
Mutation
c.289G>T
Nature of test
mutation test
FCI Number
226
GTP Breed
Landseer/ European continental type