PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

ule turnaround : 3-6 ụbọchị ma ọ bụ Express 3 ụbọchị
udiri anumanu : Abyssin, Somali
samples : Buccal swab, ma ọ bụ Blood in EDTA tube, ma ọ bụ Blood na akọrọ tube

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.

Understanding pụta nke ule: 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.
Test aha: PRA rdy - Progressive Retinal Atrophy
Gene mutation: CRX n.546delC
si n'aka ruo n'aka: autosomal dominant (ozi ọzọ)
Penetrance: complete (ozi ọzọ)
Test N'ihiPRA rdy - Progressive Retinal Atrophy ọnọdụ (CRX n.546delC)Health ọnọdụ
N/NNo copy of the PRA rdy mutationAnimal nkịtị (ikpochapụ)
PRA rdy/N1 copy of the PRA rdy mutationAnimal bụ, ga-ma ọ bụ nwere ike na-emetụta
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal bụ, ga-ma ọ bụ nwere ike na-emetụta

Cross table nke ule: PRA rdy - Progressive Retinal Atrophy


nne N/Nnne PRA rdy/Nnne PRA rdy/PRA rdy
Nna N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Nna 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
Nna PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Certificate atụ maka ule: PRA rdy - Progressive Retinal Atrophy

Pịa na atụ akwụkwọ n'okpuru imeghe ya.

Certificate

References

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.

Nyocha

E nweghị ndị na reviews ma.

Naanị ite ke ahịa ndị zụrụ ngwaahịa a pụrụ ịhapụ a nyochaa.