{"id":1332703,"date":"2020-10-16T11:36:27","date_gmt":"2020-10-16T09:36:27","guid":{"rendered":"https:\/\/laboklin.de\/leistungen\/genetik\/erbkrankheiten\/katze\/"},"modified":"2025-02-25T12:06:43","modified_gmt":"2025-02-25T11:06:43","slug":"katze","status":"publish","type":"page","link":"https:\/\/laboklin.de\/de-at\/leistungen\/genetik\/erbkrankheiten\/katze\/","title":{"rendered":"Katze"},"content":{"rendered":"

[vc_row][vc_column][vc_column_text]Wir bieten Genetikpakete<\/a> f\u00fcr die Untersuchung mehrerer Erbkrankheiten an.[\/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]

Leistungsspektrum<\/h3>
  • Acrodermatitis enteropathica (AE)<\/a><\/li>
  • Alpha-Mannosidose (AMD)<\/a><\/li>
  • Autoimmunes lymphoproliferatives Syndrom (ALPS)<\/a><\/li>
  • Blau\u00e4ugigkeit<\/a><\/li>
  • Blutgruppenbestimmung genetisch<\/a><\/li>
  • Blutgruppenbestimmung serologisch (Hund, Katze)<\/a><\/li>
  • Congenitale Hypothyreose (CH)<\/a><\/li>
  • Congenitales myasthenes Syndrom (CMS)<\/a><\/li>
  • Cystinurie<\/a><\/li>
  • Faktor XI-Defizienz (F11)<\/a><\/li>
  • Faktor XII-Defizienz (F12)<\/a><\/li>
  • Gangliosidose (GM1)<\/a><\/li>
  • Gangliosidose (GM2)<\/a><\/li>
  • Gangliosidose (GM2)<\/a><\/li>
  • Glycogenspeicherkrankheit Typ 4 (GSD4)<\/a><\/li>
  • Head defect<\/a><\/li>
  • Hypertrophe Kardiomyopathie (HCM1)<\/a><\/li>
  • Hypertrophe Kardiomyopathie (HCM3)<\/a><\/li>
  • Hypertrophe Kardiomyopathie (HCM4)<\/a><\/li>
  • Hypokali\u00e4mie<\/a><\/li>
  • Hypotrichose und Kurzlebigkeit<\/a><\/li>
  • MDR1-Genvariante<\/a><\/li>
  • Mukopolysaccharidose Typ VI (MPS6)<\/a><\/li>
  • Mukopolysaccharidose Typ VII (MPS7)<\/a><\/li>
  • Myotonia congenita<\/a><\/li>
  • Osteochondrodysplasie (OCD)<\/a><\/li>
  • Polydaktylie<\/a><\/li>
  • Polyzystische Nierenerkrankung (PKD)<\/a><\/li>
  • Polyzystische Nierenerkrankung (PKD2)<\/a><\/li>
  • Prim\u00e4res erbliches Glaukom (PCG)<\/a><\/li>
  • Progressive Retinaatrophie (b-PRA)<\/a><\/li>
  • Progressive Retinaatrophie (pd-PRA)<\/a><\/li>
  • Progressive Retinaatrophie (rdAc-PRA)<\/a><\/li>
  • Progressive Retinaatrophie (rdy-PRA)<\/a><\/li>
  • Pyruvatkinase-Defizienz (PK)<\/a><\/li>
  • Skeletale Dysplasie (SD)<\/a><\/li>
  • Spinale Muskelatrophie (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]Wir bieten Genetikpakete f\u00fcr die Untersuchung mehrerer Erbkrankheiten an.[\/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][\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1332679,"menu_order":1,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_robots_primary_cat":"","_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","footnotes":""},"class_list":["post-1332703","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/pages\/1332703","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/comments?post=1332703"}],"version-history":[{"count":1,"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/pages\/1332703\/revisions"}],"predecessor-version":[{"id":1428114,"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/pages\/1332703\/revisions\/1428114"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/pages\/1332679"}],"wp:attachment":[{"href":"https:\/\/laboklin.de\/de-at\/wp-json\/wp\/v2\/media?parent=1332703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}