PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

ho'āʻo ma turnaround : 3-6 lā a me Express 3 lā
Breeds : Abyssin, Somali
Eia kekahi laʻana : Buccal swab, a me ke koko i loko o EDTA şarkı, a me kou Koko i ka maloo Tube

Mea
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali mahele:
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.

Hoʻomaopopo i nā hualoaʻa o ka hoʻokolohua. 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.
Ninau hoopoipoi inoa: PRA rdy - Progressive Retinal Atrophy
'Ōewe Mutation: CRX n.546delC
nā kūpuna mai: autosomal Hoʻohaku (hou 'ike)
Penetrance: piha (hou 'ike)
hoʻokolohua hopenaPRA rdy - Progressive Retinal Atrophy kūlana (CRX n.546delC)Health you
N/NNo copy of the PRA rdy mutationAnimal mea maʻamau (moakaka)
PRA rdy/N1 copy of the PRA rdy mutationAnimal mea, e 'ole hiki ke loli
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal mea, e 'ole hiki ke loli

Keʻa papa o ka hoʻokolohua. PRA rdy - Progressive Retinal Atrophy


Makuahine N/NMakuahine PRA rdy/NMakuahine PRA rdy/PRA rdy
Makuakāne N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Makuakāne 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
Makuakāne PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Palapala laʻana no ka hoao ana: PRA rdy - Progressive Retinal Atrophy

E kaomi ma luna o ka hana palapala ma lalo nei, e wehe ia.

palapala

E hoʻomaopopo '

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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