PRA rdy – Progressive Jeexitaanka atrophy

44,90

Specific to Abyssin, Somali breeds

imtixaanada gudbay : 3-6 maalmood ama Express 3 maalmood
eyda : Abyssin, Somali
Muunado : Suuf loogu talagalay, ama dhiigga ee tube EDTA, ama dhiigga ee tube qalalan

Clear
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali Category:
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.

Fahamka natiijooyinka imtixaanka: 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.
Magaca Test: PRA rdy - Progressive Retinal Atrophy
Gene isbedel: CRX n.546delC
hiddo: autosomal xukuma (macluumaad intaas ka badan)
Penetrance: complete (macluumaad intaas ka badan)
natiijada imtixaankaPRA rdy - Progressive Retinal Atrophy status (CRX n.546delC)xaalada caafimaadka
N/NNo copy of the PRA rdy mutationXoolaha waa caadi (cad)
PRA rdy/N1 copy of the PRA rdy mutationXoolaha waa, doonaa ama waxyeelayn karaan
PRA rdy/PRA rdy2 copies of the PRA rdy mutationXoolaha waa, doonaa ama waxyeelayn karaan

miiska Cross imtixaanka: PRA rdy - Progressive Retinal Atrophy


Hooyo N/NHooyo PRA rdy/NHooyo PRA rdy/PRA rdy
Aabbaha N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Aabbaha 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
Aabbaha PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Certificate tusaale ahaan imtixaanka: PRA rdy - Progressive Retinal Atrophy

Riix tusaale ahaan shahaadada hoose si aad u furto.

shahaadada

tixraacyada

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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