PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Toetse omkeer : 3-6 dae of druk 3 dae
Rasse : Abyssin, Somali
Monsters : Buccal depper, of bloed in EDTA Tube, of bloed in droë buis

Duidelik
SKU pra-rdy-progressive-retinal-atrophy-abyssin-somali Kategorie:
N/N : Normal, no copy of the PRA rdy mutation. N/PRA rdy : one copy of the PRA rdy mutation, the cat may develop this disease. PRA rdy/PRA rdy : 2 copies of the PRA rdy mutation, the cat may develop this disease.

What is PRA rdyProgressive Retinal Atrophy?

PRA rdyProgressive Retinal Atrophy is a specific mutation found in Abyssin and Somali cat. This disease produce rod cone dysplasia. Kittens will be blind at around 7 weeks old due to a defective protein which is needed for the normal eye development.

Verstaan resultate van die toets: PRA rdy - Progressive Retinal Atrophy


N/N : Normal, no copy of the PRA rdy mutation. N/PRA rdy : one copy of the PRA rdy mutation, the cat may develop this disease. PRA rdy/PRA rdy : 2 copies of the PRA rdy mutation, the cat may develop this disease.
Toets naam: PRA rdy - Progressive Retinal Atrophy
Geenmutasie: CRX n.546delC
Oorerwing: autosomal dominant (meer inligting)
Penetrance : complete (meer inligting)
ToetsuitslagPRA rdy - Progressive Retinal Atrophy statusCRX n.546delC)Gesondheidstatus
N/NNo copy of the PRA rdy mutationDier is normaal (duidelik)
PRA rdy/N1 copy of the PRA rdy mutationAnimal is, will or could be affected
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal is, will or could be affected

Cross table of the test : PRA rdy - Progressive Retinal Atrophy


Mother N/NMother PRA rdy/NMother PRA rdy/PRA rdy
Father N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Father PRA rdy/N50% N/N
50% PRA rdy/N
25% N/N
50% PRA rdy/N
25% PRA rdy/PRA rdy
50% PRA rdy/N
50% PRA rdy/PRA rdy
Father PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Certificate example for the test : PRA rdy - Progressive Retinal Atrophy

Click on the example certificate below to open it.

Sertifikaat

References

Menotti-Raymond M, Deckman KH, David V, Myrkalo J, O’Brien SJ, Narfström K. Mutation discovered in a feline model of human congenital retinal blinding disease. Invest Ophthalmol Vis Sci. 2010 Jun; 51(6):2852-9. Epub 2010 Jan 6. PubMed PMID: 20053974.

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