RCD4
Progressive retinal atrophy
| Nimi: | Progressive Retinal Atrophy (rcd4-PRA) |
|---|---|
| Geenin sijainti: | PCARE |
| Kromosomi: | 17 |
| Mutaatio: | c.3149_3150insC |
| Oireyhtymä: | Oftamologinen |
| Periytymismekanismi: | Autosomaalisesti resessiivinen |
| Testityyppi: | Suora mutaatiotesti |
| Tyypillinen sairastumisikä: | ~10 years |
Huom. Yllä olevat tiedot koskevat tiibetinterriereillä esiintyvää geeniä.
| Yleistä tietoa | ||||
|---|---|---|---|---|
The Progressive Retinal Atrophy (PRA) leads to a degeneration of the retina and results in blindness. The Rod-cone-dysplasia type 4 (rcd4)-PRA is characterised as a Late Onset PRA (LOPRA). Night blindness is a typical first symptom of the disease. However, not all ophthalmological PRA-affected Tibetan Terriers could be explained by RCD4. Therefore, additional unknown PRA causing variants are suspected besides to the PRA3 & rcd4-PRA variants in Tibetan Terriers. | ||||
| Kliiniset oireet | ||||
|---|---|---|---|---|
Otathan huomioon, että oireet ja ikäarviot voivat vaihdella ja poiketa myös edellä mainituista. | ||||
| Sairastavuus | |||
|---|---|---|---|
CLEAR / N/N ![]() | CLEAR / N/N = Dogs with N/N genotype will not have this variant of PRA. If N/N dog is affected by PRA, it’s different PRA-gene or unknown mutation. | ||
CARRIER / N/RCD4 ![]() | CARRIER / N/RCD4 = Dogs with N/RCD4 genotype are generally clinically healthy and do not develop the disease. If N/RCD4 dog is affected by PRA, it’s different PRA-gene or unknown mutation. | ||
AFFECTED / RCD4/RCD4 ![]() | AFFECTED / RCD4/RCD4 = Dogs with RCD4/RCD4 dogs appear normal at birth, but begin to exhibit clinical effects later. Symptoms often appear between around 5-12 years of age. The age of onset of the disease can vary greatly among individuals. | ||
| Periytyminen | |
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