{"id":228713,"date":"2024-09-12T07:23:54","date_gmt":"2024-09-12T05:23:54","guid":{"rendered":"http:\/\/staging.laboklin.com\/labogen\/labogen_wp\/paket-perser"},"modified":"2024-09-12T07:23:54","modified_gmt":"2024-09-12T05:23:54","slug":"paket-perser","status":"publish","type":"page","link":"https:\/\/labogen.com\/uk\/pakete-testkombinationen-katze\/paket-perser\/","title":{"rendered":"Paket Perser"},"content":{"rendered":"

Combination Persian<\/h1>

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

includes: Alpha-Mannosidosis (AMD), genetic blood group testing, Polycystic kidney disease (PDK) and Progressive retinal atrophy (pd-PRA) <\/p>

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

Persian<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8713<\/td><\/tr>
Sample material<\/strong><\/td>0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)<\/td><\/tr>
Test duration<\/strong><\/td>7-14 working days<\/td><\/tr><\/table><\/details><\/div>
Order now ...<\/a><\/strong><\/div><\/div><\/div>
<\/div><\/div>

Progressive retinal atrophy (pd-PRA)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>ophthalmic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>5 weeks <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>AIPL1<\/td><\/tr>
Mutation<\/strong><\/td>C-T<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001222-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Alpha-Mannosidosis (AMD)<\/h4><\/div>
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>MAN2B1<\/td><\/tr>
Mutation<\/strong><\/td>DEL<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000625-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Polycystic kidney disease (PKD)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>nephrological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal dominant<\/td><\/tr>
Age of onset<\/strong><\/td>8 months<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>PKD1<\/td><\/tr>
Mutation<\/strong><\/td>C-A<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000807-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Genetic blood group <\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>hematologic<\/td><\/tr>
Inheritance<\/strong><\/td>Allelische Reihe nach Dominanz: N>c>b<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>CMAH<\/td><\/tr>
Mutation<\/strong><\/td>COMPLEX<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000119-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
 <\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":1,"featured_media":0,"parent":10714,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-228713","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/pages\/228713","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/comments?post=228713"}],"version-history":[{"count":0,"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/pages\/228713\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/pages\/10714"}],"wp:attachment":[{"href":"https:\/\/labogen.com\/uk\/wp-json\/wp\/v2\/media?parent=228713"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}