PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

mayesero kutembenuza : Masiku 3-6 kapena Express 3 masiku
Kubweretsa : Abyssin, Somali
poonekera : Buccal swab, kapena magazi EDTA chubu kapena magazi chubu youma

Chotsani
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.

Kumvetsa Zotsatila zake: 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.
dzina mayeso: PRA rdy - Progressive Retinal Atrophy
Gene Kafukufuku: CRX n.546delC
chibadwa: autosomal lalikulu (zambiri)
Penetrance: wathunthu (zambiri)
chifukwa mayesoPRA rdy - Progressive Retinal Atrophy udindo wake (CRX n.546delC)udindo Health
N/NNo copy of the PRA rdy mutationAnimal yachibadwa (poyera)
PRA rdy/N1 copy of the PRA rdy mutationAnimal, kodi kapena idzakhudzidwa
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal, kodi kapena idzakhudzidwa

Cross tebulo la mayeso: PRA rdy - Progressive Retinal Atrophy


amayi N/Namayi PRA rdy/Namayi PRA rdy/PRA rdy
Atate N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Atate 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
Atate PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Mwachitsanzo satifiketi mayeso: PRA rdy - Progressive Retinal Atrophy

Dinani pa satifiketi chitsanzo chiri musichi kutsegula izo.

Certificate

Zothandizira

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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