Glykogen storage disease GSDIIIa

Order number: GSD169
€48.79

VAT incl.

Application: - Carrier identification - Differential diagnosis. With this test we investigate if the dog carries a mutation in the AGL-gene that was described as the cause of Glycogen Storage Disease (GSD) type IIIa in Curly Coated Retrievers. In their early years symptoms often cannot be recognized. But later they progress and affected dogs are lethargic, show exercise intolerance and... more
Product information "Glykogen storage disease GSDIIIa"
Application:
- Carrier identification
- Differential diagnosis.
With this test we investigate if the dog carries a mutation in the AGL-gene that was described as the cause of Glycogen Storage Disease (GSD) type IIIa in Curly Coated Retrievers.
In their early years symptoms often cannot be recognized. But later they progress and affected dogs are lethargic, show exercise intolerance and episodic hypoglycaemia with collapse/unresponsiveness.
The disease is inherited in an autosomal recessive manner, only dogs with two mutated alleles are affected.
In the lexicon you will find more information and explanations about the article more
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Classification:
Species: Dog
Type: DNA tests
Class: Inherited diseases
Breeding clubs: Deutscher Retriever Club e.V., DRC. DNA-Programm Identität und Eigenschaften
Breed: Curly Coated Retriever, Mischling Hund, Sonstige, unbekannt, verschiedene Rassen
Group: Metabolism
Package Coat Color Retriever (P5)
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A – Locus / Agouti - DOG
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B – Locus (Coat color 'Brown' - DOG)
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Centronuclear Myopathy (CNM)
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crd-PRA
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Curly Coat
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D – Locus (Dilution)
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Cerebellar hypoplasia (Dandy Walker Like...
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E – Locus (Coat color 'Yellow')
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Furnishings
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Golden Retriever PRA 1
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Golden Retriever PRA 2
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Harlequin coat pattern
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L – Locus (hair length)
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K – Locus (dominant black)
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Malignant Hyperthermia - DOG
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Merle coat pattern
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Narcolepsy (Dachshund)
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Narcolepsia (Dobermann)
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Narcolepsy (Labrador)
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Neuronal Ceroid-Lipofuscinosis 1 (Dachshund)
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Neuronal Ceroid-Lipofuscinosis 2 (Dachshund)
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Neuronal Ceroid-Lipofuscinosis 5 (Golden...
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Osteogenesis Imperfecta (Dachshund)
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S – Locus (Piebald)
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Skeletal Dysplasia 2
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Von-Willebrand-Disease Type 1
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Golden Retriever muscular dystrophy
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Cystinuria-A (Newfoundland)
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Cone-rod dystrophy 4 - Progressive Retinal...
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Juvenile Myoclonic Epilepsy
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CDDY & IVDD
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prcd-PRA***
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HNPK
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Exercise Induced Collapse (EIC)***
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Ichtyosis (ICT-A)***
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Collie eye anomaly (CEA)***
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RD_OSD***
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STGD - Stargardt Disease
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Hämophilie B [p]
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Malignant Hyperthermia - HORSE
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Polysaccharide Storage Myopathy 1 (PSSM1***)
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DNA profile Identity DOG (ISAG-22-Marker)
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DNA profile Identity DOG - *** class, extended...
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Neuronal Ceroid Lipofuscinosis 10 (NCL10)
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Em – Locus (melanistic mask)
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Hyperuricosuria
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Hereditary Equine Regional Dermal Asthenia (HERDA)
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Hyperkalemic Periodic Paralysis (HYPP)
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Junctional Epidermolysis Bullosa (JEB)
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Generalized Progressive Retinal Atrophy (gPRA)
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Cone-rod dystrophy 1 (crd-1)
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Myotubular Myopathy (X-linked)
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Cystinuria II-B
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Ectodermal Dysplasia
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Glycogen Branching Enzyme Deficiency (GBED)
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Canine Multifocal Retinopathy 1 (cmr1)
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