PRA rdyProgressive Retinal Atrophy

44, 90

Specific to Abyssin, Somali breeds

Testi preobrata : 3-6 dni ali Express 3 dni
Pasme : Abyssin, Somali
Vzorcev : Buccal zloženec ali kri v epruveti EDTA ali kri v suhi cevi

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.

Razumevanje rezultatov preskusa: 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.
Preizkusno ime: PRA rdy - Progressive Retinal Atrophy
Genske mutacije: CRX n.546delC
Dednosti: autosomal dominant (več informacij)
Penetrance complete (več informacij)
Rezultat testaPRA rdy - Progressive Retinal Atrophy statusCRX n.546delC)Zdravstveno stanje
N/NNo copy of the PRA rdy mutationŽival je normalna (Bistra)
PRA rdy/N1 copy of the PRA rdy mutationŽival je, bo ali bi lahko vplivala
PRA rdy/PRA rdy2 copies of the PRA rdy mutationŽival je, bo ali bi lahko vplivala

Navzkrižna preglednica preskusa: PRA rdy - Progressive Retinal Atrophy


Mati N/NMati PRA rdy/NMati PRA rdy/PRA rdy
Oče N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Oče 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
Oče PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Primer certifikata za preskus: PRA rdy - Progressive Retinal Atrophy

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Potrdilo

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.

Napišejo

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