{"id":1421759,"date":"2020-10-16T11:36:27","date_gmt":"2020-10-16T09:36:27","guid":{"rendered":"https:\/\/staging-wp-int.laboklin.com\/products\/genetics\/hereditary-diseases\/cat\/"},"modified":"2022-11-21T19:49:29","modified_gmt":"2022-11-21T18:49:29","slug":"cat","status":"publish","type":"page","link":"https:\/\/laboklin.com\/dk\/products\/genetics\/hereditary-diseases\/cat\/","title":{"rendered":"Cat"},"content":{"rendered":"

[vc_row][vc_column][vc_column_text][\/vc_column_text][\/vc_column][\/vc_row][vc_row type=”vc_default” css=”.vc_custom_1612193384899{margin-top: 30px !important;}”][vc_column][vc_column_text]We also offer genetic test combinations<\/a> to test for several hereditary diseases. Please contact us, we will be happy to advise you.<\/p>\n

<\/div>\n

Diagnostic spectrum<\/h3>
  • Acrodermatitis enteropathica (AE)<\/a><\/li>
  • Alpha-Mannosidosis (AMD)<\/a><\/li>
  • Atherosclerosis (ATH)<\/a><\/li>
  • Autoimmune lymphoproliferative syndrome (ALPS)<\/a><\/li>
  • Genetic blood group determination<\/a><\/li>
  • Serological Blood Group Typing (dog, cat)<\/a><\/li>
  • Blue eyes<\/a><\/li>
  • Congenital hypothyroidism (CH)<\/a><\/li>
  • Congenital myasthenic syndrome (CMS)<\/a><\/li>
  • Cystinuria<\/a><\/li>
  • Epileptic encephalopathy (EE)<\/a><\/li>
  • Factor XI deficiency (F11)<\/a><\/li>
  • Factor XII deficiency (F12)<\/a><\/li>
  • Gangliosidosis (GM1)<\/a><\/li>
  • Gangliosidosis (GM2)<\/a><\/li>
  • Gangliosidosis (GM2)<\/a><\/li>
  • Glycogen storage disease type 4 (GSD4)<\/a><\/li>
  • Head defect<\/a><\/li>
  • Hypertrophic cardiomyopathy (HCM1)<\/a><\/li>
  • Hypertrophic cardiomyopathy (HCM3)<\/a><\/li>
  • Hypertrophic cardiomyopathy (HCM4)<\/a><\/li>
  • Hypokalaemia<\/a><\/li>
  • Hypotrichosis and short life expectancy<\/a><\/li>
  • MDR1 gene variant<\/a><\/li>
  • Mucopolysaccharidosis type VI (MPS6)<\/a><\/li>
  • Mucopolysaccharidosis type VII (MPS7)<\/a><\/li>
  • Myotonia congenita<\/a><\/li>
  • Osteochondrodysplasia (OCD)<\/a><\/li>
  • Polycystic kidney disease (PKD)<\/a><\/li>
  • Polycystic kidney disease (PKD2)<\/a><\/li>
  • Primary congenital glaucoma (PCG)<\/a><\/li>
  • Progressive retinal atrophy (b-PRA)<\/a><\/li>
  • Progressive retinal atrophy (pd-PRA)<\/a><\/li>
  • Progressive retinal atrophy (rdAc-PRA)<\/a><\/li>
  • Progressive retinal atrophy (rdy-PRA)<\/a><\/li>
  • Pyruvate kinase deficiency (PK)<\/a><\/li>
  • Skeletal dysplasia (SD)<\/a><\/li>
  • Spinal muscular atrophy (SMA)<\/a><\/li><\/div><\/div>[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

    [vc_row][vc_column][vc_column_text][\/vc_column_text][\/vc_column][\/vc_row][vc_row type=”vc_default” css=”.vc_custom_1612193384899{margin-top: 30px !important;}”][vc_column][vc_column_text]We also offer genetic test combinations to test for several hereditary diseases. Please contact us, we will be happy to advise you. [\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1383322,"menu_order":1,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_robots_primary_cat":"","_seopress_titles_title":"Hereditary Diseases \u2013 Cat ENG","_seopress_titles_desc":"","_seopress_robots_index":"","footnotes":""},"class_list":["post-1421759","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/pages\/1421759","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/comments?post=1421759"}],"version-history":[{"count":0,"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/pages\/1421759\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/pages\/1383322"}],"wp:attachment":[{"href":"https:\/\/laboklin.com\/dk\/wp-json\/wp\/v2\/media?parent=1421759"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}