PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Veitarogi turnaround : 3-6 na siga se vakaraitaka e 3 na siga
Bucina : Abyssin, Somali
Sabolo eso : Buccal swab, se dra e EDTA ilumu, se dra ena mamaca ilumu

Matata
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali IWasewase
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.

Na kilai ni isau ni veivakatovolei: 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.
Yaca ni Vakatovotovo: PRA rdy - Progressive Retinal Atrophy
Gene Mutation: CRX n.546delC
Itutu autosomal dua (ikuri ni itukutuku)
Penetrance : vakacavaraikuri ni itukutuku)
Vakatovolea na isauPRA rdy - Progressive Retinal Atrophy ituvakiCRX n.546delC)Ituvaki ni bula
N/NNo copy of the PRA rdy mutationSa tu na manumanu (matata)
PRA rdy/N1 copy of the PRA rdy mutationNa manumanu e sa na rawa ni tarai
PRA rdy/PRA rdy2 copies of the PRA rdy mutationNa manumanu e sa na rawa ni tarai

Ituvatuva ni kena vakatovolei na: PRA rdy - Progressive Retinal Atrophy


Tina N/NTina PRA rdy/NTina PRA rdy/PRA rdy
Tamada N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Tamada 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
Tamada PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Ivakaraitaki ni sitivikiti ni Vakatovotovo: PRA rdy - Progressive Retinal Atrophy

Kiliki ena sitivikiti ni ivakaraitaki e ra me dolavi kina.

Sitivikiti

Veitikina

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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