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Cerebellar abiotrofi - CA

    DNA-test DNA-test for Cerebellar Abiotrophy (CA) – Rene og delavlede arabiske heste. Denne test verificerer tilstedeværelsen af ​​den recessive CA-mutation. Eksempel...

    329,00 kr

      Sample RequirementsSample Requirements

      30 to 40 - hair roots - envelope or 5 mL - blood - K3 EDTA tube

      Send your sample by regular mail or express delivery to:

      Equigerminal Lab HIESE
      Rua da Quinta do Sobreiro Nº25
      3230-343 Penela, Portugal

      Turnaround TimeTurnaround Time

      2 to 5 working days

      About the testAbout the test

      DNA test for Cerebellar Abiotrophy (CA) – Pure and part-bred Arabian horses.

      This test verifies the presence of the recessive CA mutation.

      Why test?Why test?

      This DNA test determines CA clear, carrier or affected status. Informed choices can be made for breeding selections, and prevent the born of affected foals.

      CA is sometimes confused with Wobbler’s syndrome, Equine Protozoal Myeloencephalitis (EPM) and injury-related problems, such as a concussion, so this DNA test could help on the diagnostic.

      ResultsResults

      The DNA test verifies the presence of the recessive CA mutation and presents results as one of the following:

      • N/ Negative for CA. Absence of the allele responsible for CA.
      • N/CA– Carrier - Positive heterozygous for CA. Presence of one copy of the allele responsible for CA.The horse is a carrier for CA disorder and can pass on a copy of CA allele to 50% of their progeny when bred.
      • CA/ Affected - Positive Homozygous for CA. Presence of two copies of the allele responsible for CA.The horse is affected byCA disorder and can pass the CA allele to 100% of their progeny when bred.
      Additional informationAdditional information

      Cerebellar Abiotrophy (CA) is a genetic neurological disease in certain species of animals.

      The disorder manifests itself when Purkinje cells, the neurons that affect balance and coordination, are present in the cerebellum of the brain.

      This condition is known to affect Arabian horses as well as Miniature horses, the Gotland Pony and possibly the Oldenburg.

      In most cases, foals appear normal at birth, and symptoms generally become noticeable after four months. There have been reported cases where the condition was observed shortly after birth, while others report symptoms developing after the first year.

      Horses affected with CA tend to startle easily and often fall. Common symptoms include head tremor, a lack of balance and other neurological issues.

      Affected horses may develop a wide-based stance of the forelegs and difficulty rising from a reclining position.

      In horses, CA is believed to be linked to an autosomal recessive gene. This means that it is not sex-linked and the allele has to be carried and passed on by both parents in order for an affected animal to be born.

      Horses that only carry one copy of the gene may pass it on to their offspring, despite being perfectly healthy themselves and having no symptoms of the disease.

      Because the disorder is recessive, the allele for CA may pass through multiple generations before it is expressed.

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