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Eyes
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Collie eye anomaly (CEA)***
Order number: PSD570
  • *** Partner laboratory
  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Identification of heterozygous carriers in breeding selection.
    - Differential diagnosis of eye disorders.
    Collie eye anomaly (CEA) is a developmental disorder of the eye characterised by hypoplasia (underdevelopment) of the choroid. In severe cases CEA leads to blindness. The disease occurs in Collie, Border Collie, Australian Shepherd and Shetland Sheepdog....
    cord1_crd4-PRA
    Order number: GSD361
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Identification of heterozygous carriers
    The test examines the mutation in the RPGRP1 gene, which was described in the original publication as a risk factor for cone-rod dystrophy 1-progressive retinal atrophy (crd4/cord1-PRA) in longhaired miniature dachshunds. Further research revealed that cord1 also occurs in other breeds and is a multigenic disease in...
    crd-PRA
    Order number: GSD307
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Test indication: a) Identfication of carriers among offsping of a carrier x free mating. b) Differential diagnosis of clinical PRA cases.
    crd-PRA is an early onset type of PRA described for wirehaired dachshunds. The defect occurs in the NPHP4 gene and has an autosomal-rezessive inheritance mode.
    Golden Retriever PRA 1
    Order number: GSD514
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application: - Carrier identification - Differential diagnosis in clinical PRA.
    With this test we investigate if the dog carries a mutation in the SLC4A3-gene that was identified as the cause of GR_PRA1. PRA (Progressive Retinal Atrophy) is the name for a group of diseases of the eye. They are characterised by a progressive degeneration of the retina that eventually leads...
    Golden Retriever PRA 2
    Order number: GSD515
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application: - Carrier identification - Differential diagnosis in clinical PRA.
    With this test we investigate if the dog carries a mutation in the TTC8-gene that was identified as the cause of GR_PRA2. PRA (Progressive Retinal Atrophy) is the name for a group of diseases of the eye. They are characterised by a progressive degeneration of the retina that eventually leads to...
    prcd-PRA***
    Order number: PSD566
  • *** Partner laboratory
  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application of the test:
    - Differential diagnosis in clinical PRA
    - Detection of mixed-breed, healthy carriers for breeding selection
    The tested mutation is a hereditary cause for the onset of PRA, especially in Labrador Retrievers.
    The inheritance is autosomal recessive; the hereditary disease occurs when both gene copies carry the mutation, heterozygous carriers are...
    RD_OSD***
    Order number: PSD572
  • *** Partner laboratory
  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Oculoskeletal Dysplasia 1
    *** = the test is carried out in a partner laboratory
    Please note: Due to the Corona pandemic, the processing time is up to 4-6 weeks.
    STGD - Stargardt Disease
    Order number: GSD573
    €46.41 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Identification of heterozygous carriers for breeding selection
    - Differential diagnosis in case of visual impairment
    The test examines whether the mutation (c.4176insC) in the ABCA4 gene that causes 'Stargardt Disease' (STGD) is present. The mode of inheritance is autosomal recessive, so that only animals in which both hereditary factors are defective develop...