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Musculoskeletal system
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CNM
Order number: GSD176
€48.79 VAT incl.
List price - personal prices are available after logging into ATC user account.
Application: a) Carrier identification in offspring after mating of a 'CNM-carrier' with a 'CNM-free' animal, b) Differential diagnosis in cases of clinical muscle insufficiency. Centronuclear Myopathy (CNM), also described as HMLR, or Hereditary Myopathy of Labrador Retrievers, has an autosomal recessive expression. Affected animals show insufficient muscle function...
Exercise Induced Collapse (EIC)***
Order number: PSD568
  • *** Partner laboratory
  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application of the test:
    - Identification of heterozygous, healthy carriers for breeding selection.
    - Differential diagnosis of weakness of the backhand
    The test determines whether the mutation in the DNM1 gene is present, which has been described as a risk factor for the occurrence of 'Exercise Induced Collapse', EIC. The inheritance is autosomal recessive, so that both...
    Golden Retriever muscular dystrophy
    Order number: GSD363
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Determination of the predisposition status for mating planning
    - Differential diagnosis of muscle weakness, muscle wasting
    The DMD:c.531-2A>G mutation in the DMD gene of the X chromosome of dogs is the causative factor for GRMD (X-linked Golden Retriever Muscular Dystrophy). The test investigates whether the mutation is present. The mode of inheritance is...
    IVDD-Type 1
    Order number: GSD564
    €49.98 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application
    - Assessment of hereditary predisposition to IVDD type 1 risk
    - Differential diagnosis in dogs with clinical disc herniation
    The test examines whether the dog carries the FGF4 retrogene insertion on chromosome 12. This mutation is considered a risk factor for the occurrence of Hansen type 1 disc herniation (IVDD type 1).
    The effect of the mutation is dominant...
    Osteogenesis Imperfecta (Dachshund)
    Order number: GSD195
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application: - Identification of heterozygous carriers for breeding selection.
    - Diagnosis in case of clinical symptoms
    The mutation for OI, osteogenesis imperfecta, is located in the SERPHIN1 gene. Affected animals have a disturbed collagen formation, so that bones break easily (glass bones) and heal badly. The abnormalities start at 3 weeks with pain, lameness and bone...
    Skeletal Dysplasia 2
    Order number: GSD326
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Identification of heterozygous carriers
    - Differential diagnosis of growth disorders
    The mutation in the gene COL11A2 investigated here leads to Skeletal Dysplasia 2 (SD2) in Labradors in the homozygous state. This is a mild form of disproportionate dwarfism. An affected dog may develop the typical phenotype of shortened legs with otherwise normal body size....