Neuronal Ceroid-Lipofuscinosis 2 (Dachshund)

Order number: GSD184
€48.79

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Application: - Identification of heterozygous carrier animals. - Differential diagnosis of diseases of the central nervous system. The test examines whether the c.325delC mutation, which has been identified as the cause of NCL2 disease, is present in the TTP1 gene. NCL2 (neuronal ceroidipofuscinase 2) is a disease of the central nervous system. Affected animals show perceptual difficulties... more
Product information "Neuronal Ceroid-Lipofuscinosis 2 (Dachshund)"
Application:
- Identification of heterozygous carrier animals.
- Differential diagnosis of diseases of the central nervous system.
The test examines whether the c.325delC mutation, which has been identified as the cause of NCL2 disease, is present in the TTP1 gene. NCL2 (neuronal ceroidipofuscinase 2) is a disease of the central nervous system. Affected animals show perceptual difficulties and increasing motor and cognitive impairments from around 8 months of age. The animals usually do not live beyond 1 year of age. NCL2 is inherited in an autosomal recessive manner, the disease only occurs when two mutated alleles are present.
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Animal assignment:
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Classification:
Species: Dog
Type: DNA tests
Class: Inherited diseases
Breeding clubs: Deutscher Teckelklub 1888 e.V., DTK
Breed: Kaninchenteckel Kurzhaar, Kaninchenteckel Langhaar, Kaninchenteckel Rauhaar, Mischling Hund, Sonstige, Teckel, Teckel Langhaar, Teckel Rauhaar, unbekannt, verschiedene Rassen, Zwergteckel Langhaar
Group: Nervous system
Test bundle 1 for wire-haired Dachshunds
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Test bundle 2 for wire-haired Dachshunds
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Test bundle 1 Coat Characteristics Dachshund.
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Hereditary diseases Dachshund - Bundle 1
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Centronuclear Myopathy (CNM)
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Furnishings
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Neuronal Ceroid-Lipofuscinosis 1 (Dachshund)
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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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Cystinuria-A (Newfoundland)
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Cone-rod dystrophy 1 - progressive retinal...
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Juvenile Myoclonic Epilepsy
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IVDD-Type 1
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prcd-PRA***
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HNPK
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Exercise Induced Collapse (EIC)***
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Collie eye anomaly (CEA)***
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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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Neuronal Ceroid Lipofuscinosis 10 (NCL10)
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Griscelli Type 1 like syndrome
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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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5 Panel
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Glycogen Branching Enzyme Deficiency (GBED)
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