PRA rDy – Progressiv Nethindeatrofi

44, 90

Specific to Abyssin, Somali breeds

Tests turnaround : 3-6 dage eller Express 3 dage
Racer : Abyssin, Somali
Prøver : Buccal vatpind eller blod i EDTA tube eller blod i tørrør

Klart
Sku: pra-rdy-progressive-retinal-atrophy-abyssin-somali Kategori:
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 rDy – Progressive 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.

Forståelse af resultaterne af testen: 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.
Test navn: PRA rdy - Progressive Retinal Atrophy
Genmutation: CRX n.546delC
Arvelighed: autosomal dominant (mere information)
Penetrans: complete (mere information)
Test resultatPRA rdy - Progressive Retinal Atrophy statusCRX n.546delC)Sundhedsstatus
N/NNo copy of the PRA rdy mutationDyret er normalt (klart)
PRA rdy/N1 copy of the PRA rdy mutationDyr er, vil eller kan blive påvirket
PRA rdy/PRA rdy2 copies of the PRA rdy mutationDyr er, vil eller kan blive påvirket

Kryds tabel over testen: PRA rdy - Progressive Retinal Atrophy


Mor N/NMor PRA rdy/NMor PRA rdy/PRA rdy
Far N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Far 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
Far PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Eksempel på certifikat for testen: PRA rdy - Progressive Retinal Atrophy

Klik på eksempel certifikatet nedenfor for at åbne det.

Certifikat

Referencer

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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