{"id":1332709,"date":"2020-10-16T11:36:27","date_gmt":"2020-10-16T09:36:27","guid":{"rendered":"https:\/\/laboklin.de\/leistungen\/genetik\/erbkrankheiten\/pferd\/"},"modified":"2025-02-25T12:28:36","modified_gmt":"2025-02-25T11:28:36","slug":"pferd","status":"publish","type":"page","link":"https:\/\/laboklin.de\/de-ch\/leistungen\/genetik\/erbkrankheiten\/pferd\/","title":{"rendered":"Pferd"},"content":{"rendered":"

[vc_row][vc_column][vc_column_text]F\u00fcr einige Rassen bieten wir auch rassespezifische Genetikpakete<\/a> f\u00fcr die Untersuchung mehrerer Erbkrankheiten an.[\/vc_column_text][\/vc_column][\/vc_row][vc_row type=»vc_default» css=».vc_custom_1612193473836{margin-top: 30px !important;}»][vc_column][vc_column_text]

Leistungsspektrum<\/h3>
  • Androgeninsensitivit\u00e4tssyndrom (AR1) <\/a><\/li>
  • Androgeninsensitivit\u00e4tssyndrom (AR2, AR3, AR4, AR5)*<\/a><\/li>
  • Cerebell\u00e4re Abiotrophie (CA)<\/a><\/li>
  • Distichiasis*<\/a><\/li>
  • Equine juvenile spinocerebell\u00e4re Ataxie (EJSCA)* <\/a><\/li>
  • Equine maligne Hyperthermie (EMH)<\/a><\/li>
  • Erbliche Myotonie <\/a><\/li>
  • Foal immunodeficiency syndrome (FIS)<\/a><\/li>
  • Glycogen branching enzyme deficiency (GBED)<\/a><\/li>
  • Hereditary equine regionale dermale asthenia (HERDA)<\/a><\/li>
  • Junctional epidermolysis bullosa (JEB1)<\/a><\/li>
  • Junctional epidermolysis bullosa (JEB2)*<\/a><\/li>
  • Hoof wall separation disease (HWSD)<\/a><\/li>
  • Hydrocephalus<\/a><\/li>
  • Hyperkali\u00e4mische periodische Paralyse (HYPP)<\/a><\/li>
  • Hypertriglycerid\u00e4mie-induzierte Pankreatitis (HIP)<\/a><\/li>
  • Idiopathic hypocalcaemia<\/a><\/li>
  • Immune mediated myositis & MYH1 myopathy (MYHM)<\/a><\/li>
  • Lavender Foal Syndrom (LFS)<\/a><\/li>
  • Nachtblindheit (CSNB2)*<\/a><\/li>
  • Naked Foal Syndrom (NFS)<\/a><\/li>
  • Occipitoatlantoaxial malformation (OAAM)*<\/a><\/li>
  • Ocular squamous cell carcinoma (SCC)<\/a><\/li>
  • Polysaccharid-Speicher-Myopathie Typ 1 (PSSM)<\/a><\/li>
  • Schwere kombinierte Immundefizienz (SCID)<\/a><\/li>
  • Skelettatavismus (SA)*<\/a><\/li>
  • T\u00f6dlicher wei\u00dfer Overodefekt (OLWS)<\/a><\/li>
  • Warmblood fragile foal syndrome (WFFS)<\/a><\/li>
  • Zwergwuchs<\/a><\/li>
  • Zwergwuchs (ACAN, Chondrodysplasie)<\/a><\/li><\/div><\/div>\n
    <\/div>\n

    * Partnerlabor[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

    [vc_row][vc_column][vc_column_text]F\u00fcr einige Rassen bieten wir auch rassespezifische Genetikpakete f\u00fcr die Untersuchung mehrerer Erbkrankheiten an.[\/vc_column_text][\/vc_column][\/vc_row][vc_row type=»vc_default» css=».vc_custom_1612193473836{margin-top: 30px !important;}»][vc_column][vc_column_text] * Partnerlabor[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1332680,"menu_order":2,"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-1332709","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/pages\/1332709","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/comments?post=1332709"}],"version-history":[{"count":2,"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/pages\/1332709\/revisions"}],"predecessor-version":[{"id":1456079,"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/pages\/1332709\/revisions\/1456079"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/pages\/1332680"}],"wp:attachment":[{"href":"https:\/\/laboklin.de\/de-ch\/wp-json\/wp\/v2\/media?parent=1332709"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}