PRA rdyProgressive Retinal Atrophy

44, 90

Specific to Abyssin, Somali breeds

Preokreta na testovima : 3-6 days or Express 3 days
Rađa : Abyssin, Somali
Uzorke : Buccal swab, or Blood in EDTA tube, or Blood in dry tube

Čisto
Sku: pra-rdy-progressive-retinal-atrophy-abyssin-somali Kategorija:
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.

Razumijevanje rezultata testa: 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 naziv: PRA rdy - Progressive Retinal Atrophy
Gene Mutation : CRX n.546delC
Nasljeđe autosomal dominant (više informacija)
Penetrance : complete (više informacija)
Rezultate testaPRA rdy - Progressive Retinal Atrophy statusCRX n.546delC)Zdravstveni status
N/NNo copy of the PRA rdy mutationŽivotinja je normalna (jasna)
PRA rdy/N1 copy of the PRA rdy mutationŽivotinja je, Will ili može biti pogoðen.
PRA rdy/PRA rdy2 copies of the PRA rdy mutationŽivotinja je, Will ili može biti pogoðen.

Pređi na test: PRA rdy - Progressive Retinal Atrophy


Majka N/NMajka PRA rdy/NMajka PRA rdy/PRA rdy
Otac N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Otac 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
Otac PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Primjer potvrde za test: PRA rdy - Progressive Retinal Atrophy

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Potvrda

Reference

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.

Recenzije

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