{"id":291349,"date":"2026-09-25T13:39:16","date_gmt":"2026-09-25T11:39:16","guid":{"rendered":"https:\/\/labogen.com\/malattie-ereditarie-cane\/progressive-retinal-atrophy-xl-pra-english-cocker-spaniel\/"},"modified":"2026-09-25T13:39:16","modified_gmt":"2026-09-25T11:39:16","slug":"progressive-retinal-atrophy-xl-pra-english-cocker-spaniel","status":"publish","type":"page","link":"https:\/\/labogen.com\/it\/malattie-ereditarie-cane\/progressive-retinal-atrophy-xl-pra-english-cocker-spaniel\/","title":{"rendered":"Progressive Retinal Atrophy (XL-PRA) &#8211; English Cocker Spaniel"},"content":{"rendered":"<div class=\"wrap-top\"><div class=\"wrap-left\"><h1 class=\"header-1\">Progressive retinal atrophy (XL-PRA) - English Cocker Spaniel<\/h1><h4><strong>General description<\/strong><\/h4><p class=\"bodytext\">A variant in the <em>CACNA1F<\/em> gene has been associated with another form of Progressive Retinal Atrophy (PRA) in the English Cocker Spaniel. Affected dogs show typical signs of PRA, with the first retinal changes detectable at around 3\u20134 years of age.<\/p><h4 class=\"header-4\"><strong><span>Breeds<\/span><\/strong><\/h4><p>English Cocker Spaniel<\/p><\/div><div class=\"wrap-right\"><div class=\"wrap-toggle\"><div class=\"toggle-details\"><details><summary class=\"summary-details\">Order details<\/summary><table border=\"0\"><tr><td width=\"45%\"><span><strong>Test number<\/strong><\/span><\/td><td>9153<\/td><\/tr><tr><td><strong>Abbreviation<\/strong><\/td><td>XL-PRA<\/td><\/tr><tr><td><strong>Sample material<\/strong><\/td><td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr><tr><td><strong>Test duration<\/strong><\/td><td>7-14 working days<\/td><\/tr><\/table><\/details><details><summary class=\"summary-specs\">Test specifications<\/summary><table border=\"0\"><tr><td width=\"45%\"><strong>Symptom complex<\/strong><\/td><td>ophtalmic<\/td><\/tr><tr><td width=\"45%\"><strong>Inheritance<\/strong><\/td><td>X-linked recessive<\/td><\/tr><tr><td width=\"45%\"><strong>Age of onset<\/strong><\/td><td>3-4 years<\/td><\/tr><tr><td width=\"45%\"><strong>Gene<\/strong><\/td><td>CACNA1F<\/td><\/tr><tr><td width=\"45%\"><strong>Mutation<\/strong><\/td><td>DEL<\/td><\/tr><tr><td width=\"45%\"><strong>Literature<\/strong><\/td><td><a href='https:\/\/www.omia.org\/OMIA003046\/9615\/' target='_blank'>OMIA:003046-9615<\/a><\/td><\/tr><\/table><\/details><\/div><div class=\"order-now\"><strong><a href=\"https:\/\/shop.labogen.com\/en\/guest\/order?selectedSpecies=14\">Order now ...<\/a><\/strong><\/div><\/div><\/div><div class=\"clear-both\"><\/div><\/div><div class=\"wrap-detailed\"><details><summary class=\"detail-summary\">Detailed description<\/summary><p class=\"detailed\"><p>Progressive retinal atrophies in dogs are a heterogeneous group of <strong>genetically determined eye diseases<\/strong> characterised by progressive degeneration of the retina, which can lead to a <strong>gradual deterioration of vision and ultimately blindness<\/strong>.<\/p>  <p>In the <strong>English Cocker Spaniel<\/strong>, prcd-PRA in particular has been known for many years. However, not all clinically diagnosed cases of PRA in this breed could be explained by the known variant associated with prcd-PRA. A newly described variant in the <strong><em>CACNA1F<\/em> gene<\/strong> has now been associated with another form of PRA in the English Cocker Spaniel.<\/p>  <p>In the affected English Cocker Spaniels described to date, the first typical retinal changes were detected at approximately <strong>3\u20134 years of age<\/strong>. As this is a comparatively late-onset disease, affected dogs may already have been used for breeding before clinical changes become apparent.<\/p>  <p>A genetic test can identify the genetic variant independently of the presence of clinical signs and can therefore support <strong>targeted breeding decisions<\/strong>. However, as genetic tests only detect the specific variant being tested, they do not replace regular eye examinations by a veterinarian or veterinary ophthalmologist.<\/p>  <p>The <em>CACNA1F<\/em> gene encodes the voltage-gated calcium channel Cav1.4, which plays an important role particularly in retinal nerve cells. At the terminals of photoreceptors, calcium influx enables the continuous release of neurotransmitters and is therefore essential for the transmission of visual signals. Changes in the <em>CACNA1F<\/em> gene can impair this function and lead to retinal disease.<\/p>  <p>The CACNA1F variant is inherited in an <strong>X-linked recessive<\/strong> manner. Due to this sex-linked mode of inheritance, the possible genotypes and the risk of developing the disease differ between males and females.<\/p><\/p><\/details><\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":5,"featured_media":0,"parent":269239,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-291349","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/pages\/291349","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/comments?post=291349"}],"version-history":[{"count":0,"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/pages\/291349\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/pages\/269239"}],"wp:attachment":[{"href":"https:\/\/labogen.com\/it\/wp-json\/wp\/v2\/media?parent=291349"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}