PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Tes rotation : 3-6 jou oswa eksprime 3 jou
Elve : Abyssin, Somali
Echantiyon : Buccal prelevman, oswa san nan tib EDTA, oswa san nan tib sek

Kle
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 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.

Rezilta konpreyansyon nan tes la: 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.
Non tes: PRA rdy - Progressive Retinal Atrophy
Jen Mutation: CRX n.546delC
Redite autosomal dominant (plis enfomasyon)
Penetrance : complete (plis enfomasyon)
Rezilta tesPRA rdy - Progressive Retinal Atrophy estatiCRX n.546delC)Estati sante
N/NNo copy of the PRA rdy mutationBet se nomal (kle)
PRA rdy/N1 copy of the PRA rdy mutationAnimal se, pral oswa ta ka afekte
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal se, pral oswa ta ka afekte

Kwa tab nan tes la: PRA rdy - Progressive Retinal Atrophy


Manman N/NManman PRA rdy/NManman PRA rdy/PRA rdy
Papa N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Papa 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
Papa PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Setifika egzanp pou tes la: PRA rdy - Progressive Retinal Atrophy

Klike sou setifika egzanp ki anba a pou ouvri li.

Setifika

Referans

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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