PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Ispitni preokret : 3-6 dana ili ekspresno 3 dana
Pasmina : Abyssin, Somali
Uzoraka : Bukalna obrisak ili krv u EDTA cijevi ili krv u suhoj cijevi

Jasno
Sku: pra-rdy-progressive-retinal-atrophy-abyssin-somali Kategorija:
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.

Razumijevanje rezultata testa: 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.
Naziv testa: PRA rdy - Progressive Retinal Atrophy
Mutacija gena: CRX n.546delC
Nasljedstvo: autosomatske dominantne (više informacija)
Pravilnosti potpuniviše informacija)
Rezultat testaPRA rdy - Progressive Retinal Atrophy statusCRX n.546delC)Zdravstveno stanje
N/NNo copy of the PRA rdy mutationŽivotinja je normalna (bistra)
PRA rdy/N1 copy of the PRA rdy mutationŽivotinja je, može ili može biti zahvaćena
PRA rdy/PRA rdy2 copies of the PRA rdy mutationŽivotinja je, može ili može biti zahvaćena

Križni stol testa: PRA rdy - Progressive Retinal Atrophy


Majka N/NMajka PRA rdy/NMajka PRA rdy/PRA rdy
Otac N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Otac 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
Otac PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Primjer potvrde za test: PRA rdy - Progressive Retinal Atrophy

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Certifikat

Reference

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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