{"id":292123,"date":"2026-11-03T14:32:41","date_gmt":"2026-11-03T13:32:41","guid":{"rendered":"https:\/\/labogen.com\/?page_id=292123"},"modified":"2026-11-03T14:32:42","modified_gmt":"2026-11-03T13:32:42","slug":"autoimmunes-lymphoproliferatives-syndrom-alps","status":"publish","type":"page","link":"https:\/\/labogen.com\/fi\/erbkrankheiten-hund\/autoimmunes-lymphoproliferatives-syndrom-alps\/","title":{"rendered":"Autoimmunes lymphoproliferatives Syndrom (ALPS)"},"content":{"rendered":"<div class=\"wrap-top\"><div class=\"wrap-left\"><h1 class=\"header-1\">Autoimmune lymphoprolifeative syndrome (ALPS)<\/h1><h4><strong>General description<\/strong><\/h4><p class=\"bodytext\"><p><strong>Autoimmune lymphoproliferative syndrome (ALPS)<\/strong> is an inherited disorder of the immune system. Due to a defect in programmed cell death (apoptosis), certain immune cells are not eliminated as they normally would be. This leads to an <strong>excessive accumulation of lymphocytes<\/strong>, particularly in the lymph nodes and spleen.<\/p><\/p><h4 class=\"header-4\"><strong><span>Breeds<\/span><\/strong><\/h4><p>Boerboel<\/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>9151<\/td><\/tr><tr><td><strong>Abbreviation<\/strong><\/td><td>ALPS<\/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>immunological<\/td><\/tr><tr><td width=\"45%\"><strong>Inheritance<\/strong><\/td><td>autosomal recessive<\/td><\/tr><tr><td width=\"45%\"><strong>Age of onset<\/strong><\/td><td>about 8-15 weeks<\/td><\/tr><tr><td width=\"45%\"><strong>Gene<\/strong><\/td><td>FAS<\/td><\/tr><tr><td width=\"45%\"><strong>Mutation<\/strong><\/td><td>DUP<\/td><\/tr><tr><td width=\"45%\"><strong>Literature<\/strong><\/td><td><a href='https:\/\/www.omia.org\/OMIA003045\/9615\/' target='_blank'>OMIA:003045-9615<\/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><strong>Autoimmune lymphoproliferative syndrome (ALPS)<\/strong> is a genetic disorder affecting the regulation of the immune system. Normally, immune cells that are no longer needed or are improperly regulated are selectively eliminated through programmed cell death (apoptosis). This process is essential for maintaining balance within the immune system and preventing excessive immune responses.<\/p> <p>In <strong>Boerboel<\/strong> dogs, an association has been established between a genetic variant in the <em>FAS<\/em> gene and the development of ALPS. In affected dogs, immune system regulation is disrupted, causing certain T lymphocytes to accumulate in various organs.<\/p> <p>As early as <strong>8 to 15 weeks of age<\/strong>, this leads to <strong>markedly enlarged, non-painful lymph nodes<\/strong> and a visibly <strong>enlarged abdomen due to severe enlargement of the spleen<\/strong>. In addition, <strong>other non-specific symptoms<\/strong> have been observed in affected puppies, including anaemia (a reduced red blood cell count), thrombocytopenia (a reduced platelet count), lethargy and weakness, loss of appetite, recurrent diarrhoea, fever, and occasionally abnormal breathing sounds and coughing. The severity of clinical signs may vary.<\/p> <p>As the enlargement of the lymph nodes and changes in the lymphocyte population can resemble lymphoma, a thorough veterinary examination is required.<\/p> <p>The genetic variant is a <strong>duplication in the <em>FAS<\/em> gene<\/strong>, which encodes the FAS receptor (CD95), a protein that plays a central role in initiating programmed cell death in immune cells. The variant is inherited in an <strong>autosomal recessive<\/strong> manner.<\/p> <p>Genetic testing enables the identification of the described variant regardless of whether clinical signs are present. This allows clinically healthy carriers to be identified and taken into account in breeding decisions. In the case of recessively inherited disorders, carriers do not necessarily need to be excluded from breeding, provided they are only mated with genetically clear dogs.<\/p><\/p><\/details><\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":5,"featured_media":0,"parent":6261,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-292123","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/pages\/292123","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/comments?post=292123"}],"version-history":[{"count":1,"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/pages\/292123\/revisions"}],"predecessor-version":[{"id":292124,"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/pages\/292123\/revisions\/292124"}],"up":[{"embeddable":true,"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/pages\/6261"}],"wp:attachment":[{"href":"https:\/\/labogen.com\/fi\/wp-json\/wp\/v2\/media?parent=292123"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}