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Musculature
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PSSM2 - P8, K1 extension
Order number: GCH129

  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    PSSM2 Equine Myopathy extension panel - P8 and K1. This panel is available for horses which have already been tested for the original four EquiSeq mutations (P2, P3, P4, Px).
    This test detects variants in the genes PYROXD1 (P8) and COL6A3 (K1).
    PSSM2 6 Variant Panel
    Order number: GCH108

  • €327.25 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    PSSM2 is an umbrella term for a group of muscle diseases with symptoms that can include exercise intolerance, muscle atrophy, intermittent lameness, muscle stiffness, gait abnormalities, and pain-related behavioural changes.
    The PSSM2 Equine Myopathy Panel tests six variants associated with PSSM2: P2, P3, P4, Px, P8, K1. The test is patented by EquiSeq Inc. and is offered in...
    PSSM2-3Var. (Islandpferd)
    Order number: GCH130

  • €136.85 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    PSSM2 Equine Myopathy Panel - Icelandic Horses (P3, P8, K1). This panel is available only to Icelandic horses. The panel tests the only three PSSM2 variants known to occur in Icelandic Horses.
    Congenital Myotonia
    Order number: GSH109
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Congenital Myotonia leads to impaired movement due to muscle rigidity. It is autosomal recessive and is found in New Forest ponies and other ponies with the stallion "Kantje's Ronaldo" in the pedigree.
    Glycogen Branching Enzyme Deficiency (GBED)
    Order number: GSH103
    €49.98 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    This test detects the c.102C>A mutation in GBE1 that causes Glycogen Branching Enzyme Deficiency in Quarter Horses and related breeds. The inheritance is autosomal recessive so only animals with two defective copies (gbed/gbed) will be affected
    Hyperkalemic Periodic Paralysis (HYPP)
    Order number: GSH107
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    This test detects the c.4248C>G mutation in the SCN4A gene which causes Hyperkalemic Periodic Paralysis in Quarter Horses and related breeds (Impressive-bred). The inheritance is incomplete autosomal dominant. Animals with one (n/HYPP) or two (HYPP/HYPP) copies of the mutation will be affected.
    Malignant Hyperthermia - HORSE
    Order number: GSH110
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Malignant Hyperthermia is an autosomal dominant mutation where fever, muscle rigidity and respiratory distress and even death can be triggered by specific anaesthetics or other stress/exercise. It also worsens the symptoms of horses with PSSM1 and 2.
    Polysaccharide Storage Myopathy 1 (PSSM1***)
    Order number: PSH128
  • *** Partner laboratory
  • €49.98 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    PSSM1 is a form of exercise intolerance in which a disorder of the sugar metabolism of the muscles causes muscle damage.
    The test detects the mutation (c.926G>A) in the GYS1 gene which causes PSSM1. The inheritance is incomplete autosomal dominant. Horses with one or two copies of the genetic variant (n/P1 or P1/P1) are at risk to develop symptoms of PSSM1; those with two...