Muscular Dystrophy (Duchenne-type, DMD) GRMD
Breed: Australian Cobberdog
Generic Phene Data
Breeds
Relevance Rating: There is some evidence or research available for these breeds
General
Disease Name
Muscular Dystrophy (Duchenne-type, DMD) GRMD
OMIA
1081
Gene Name
DMD
Mutation
A>G intron 6 splice acceptor site
Mutation 2
c.7293+5G>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
Sharp, N.J.H., Kornegay, J.N., Van Camp, S.D., Herbstreith, M.H., Secore, S.L., Kettle, S.A., Hung, W.Y., Constantinou, C.D., Dykstra, M.J., Roses, A.D. and Bartlett, R.J., 1992. An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy. Genomics, 13(1), pp.115-121.
Published 2
Walmsley, GL., Arechavala-Gomeza, V., Fernandez-Fuente, M., Burke, MM., Nagel, N., Holder, A., Stanley, R., Chandler, K., Marks, SL., Muntoni, F., Shelton, GD., Piercy, RJ.: A duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping. PLoS One 5:e8647, 2010. Pubmed reference: 20072625. DOI: 10.1371/journal.pone.0008647
Body/System/Process
Muscular
OMIA Url
Inheritance
XR
Breed Specific Info
Researched Breeds
Golden Retriever
HSP Test-Specific Data
Agrotis S.r.l.
GTP
GTP Name
Agrotis S.r.l.
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
BioBank AS
GTP
GTP Name
BioBank AS
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
Certagen GmbH
GTP
GTP Name
Certagen GmbH
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
CMSCH
GTP
GTP Name
CMSCH
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
INNO
GTP
GTP Name
INNO
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
Laboratorios Labocor S.L.
GTP
GTP Name
Laboratorios Labocor S.L.
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
Paw Print Genetics
GTP
GTP Name
Paw Print Genetics
Breed
OMIA
GTP Disease Name
GRMD: Muscular Dystrophy, Duchenne type or Golden Retriever Muscular Dystrophy (GRMD)
Gene Name
DMD
Mutation
Point Mutation
Nature of test
mutation test
FCI Number
-27
PharmaDNA
GTP
GTP Name
PharmaDNA
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
Progènes-ADN
GTP
GTP Name
Progenes ADN
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
VHL Genetics
GTP
GTP Name
VHL Genetics
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation
Zoolyx
GTP
GTP Name
Zoolyx
Breed
OMIA
Gene Name
DMD
Mutation
Point Mutation