{"id":272975,"date":"2024-09-12T07:23:59","date_gmt":"2024-09-12T05:23:59","guid":{"rendered":"https:\/\/staging.laboklin.com\/labogen\/labogen_wp\/index.php\/maladies-hereditaires-chien\/larynxparalysis-with-polyneuropathy-type-3-lppn3\/"},"modified":"2024-09-12T07:23:59","modified_gmt":"2024-09-12T05:23:59","slug":"larynxparalysis-with-polyneuropathy-type-3-lppn3","status":"publish","type":"page","link":"https:\/\/labogen.com\/fr\/maladies-hereditaires-chien\/larynxparalysis-with-polyneuropathy-type-3-lppn3\/","title":{"rendered":"Larynxparalysis with polyneuropathy type 3 (LPPN3)"},"content":{"rendered":"

Larynxparalysis with polyneuropathy type 3 (LPPN3)<\/h1>

General description<\/strong><\/h4>

Dogs affected by LPPN3 often show breathing difficulties as the first sign noticed by loud and gagging breathing and leading to laryngeal paralysis. Other typical signs of a polyneuropathy such as gait disorders can also occur.<\/p>

Breeds<\/span><\/strong><\/h4>

Australian-Labradoodle (Cobberdog), Great Dane, Labradoodle, Labrador Retriever, Leonberger, St. Bernard <\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8685<\/td><\/tr>
Abbreviation<\/strong><\/td>LPPN3<\/td><\/tr>
Sample material<\/strong><\/td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr>
Test duration<\/strong><\/td>3-5 working days<\/td><\/tr><\/table><\/details>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>CNTNAP1<\/td><\/tr>
Mutation<\/strong><\/td>C-T<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002301-9615<\/a><\/td><\/tr><\/table><\/details><\/div>
Order now ...<\/a><\/strong><\/div><\/div><\/div>
<\/div><\/div>
Detailed description<\/summary>

Dogs affected by LPPN3 often show breathing difficulties as the first sign noticed by loud and gagging breathing and leading to laryngeal paralysis. Other typical signs of a polyneuropathy such as gait disorders can also occur. In addition to this mutation, there are other causal mutations that lead to the similar diseases LPN1 or LPN2 in Leonberger.<\/p><\/details><\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":1,"featured_media":0,"parent":269880,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-272975","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/272975","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/comments?post=272975"}],"version-history":[{"count":0,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/272975\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/269880"}],"wp:attachment":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/media?parent=272975"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}