PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

liteko fetola maikutlo a ka : Matsatsi a 3-6 kapa Express 3 matsatsi a
ntseng e tsoela pele : Abyssin, Somali
disampole : Buccal swab kapa Mali ka EDTA tube, kapa Mali ka lethopo omileng

hlakile
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.

Ho utloisisa liphello tsa tlhahlobo: 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.
lebitso teko: PRA rdy - Progressive Retinal Atrophy
Gene phetoho liphatseng tsa lefutso: CRX n.546delC
lefutso: autosomal ka sehloohong (boitsebiso bo eketsehileng)
Penetrance: ka ho feletseng (boitsebiso bo eketsehileng)
lebaka tekoPRA rdy - Progressive Retinal Atrophy boemo ba (CRX n.546delC)boemo ba bophelo bo botle
N/NNo copy of the PRA rdy mutationPhoofolo tloaelehileng (hlakile)
PRA rdy/N1 copy of the PRA rdy mutationPhoofolo e, e tla kapa ba ne ba ka ameha
PRA rdy/PRA rdy2 copies of the PRA rdy mutationPhoofolo e, e tla kapa ba ne ba ka ameha

Cross tafole ea teko eo: PRA rdy - Progressive Retinal Atrophy


Mother N/NMother PRA rdy/NMother PRA rdy/PRA rdy
ntate N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
ntate 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
ntate PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Mohlala lengolo la bakeng sa teko ea: PRA rdy - Progressive Retinal Atrophy

Tobetsa ka lengolo mohlala tlase ho bula e.

lengolo

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.

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