{"id":274621,"date":"2024-09-12T07:24:01","date_gmt":"2024-09-12T05:24:01","guid":{"rendered":"https:\/\/staging.laboklin.com\/labogen\/labogen_wp\/index.php\/paquets-combinaisons-de-tests-chien\/combination-border-collie\/"},"modified":"2024-09-12T07:24:01","modified_gmt":"2024-09-12T05:24:01","slug":"combination-border-collie","status":"publish","type":"page","link":"https:\/\/labogen.com\/fr\/paquets-combinaisons-de-tests-chien\/combination-border-collie\/","title":{"rendered":"Combination Border Collie"},"content":{"rendered":"

Combination Border Collie<\/h1>

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

includes: Collie eye anomaly (CEA), Glaucoma and goniodysgenesis (GG), Imerslund-Gr\u00e4sbeck syndrome (IGS), MDR1-gene defect (MDR1), Neuronal ceroid lipofuscinosis (NCL) Raine syndrome, Trapped neutrophil syndrome (TNS), Sensory neuropathy (SN)<\/p>

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

Border Collie<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8626<\/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>

Sensory neuropathy (SN)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>2-7 months <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>FAM134B<\/td><\/tr>
Mutation<\/strong><\/td>COMPLEX<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002032-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Trapped neutrophil syndrome (TNS)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>immunological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>VPS13B<\/td><\/tr>
Mutation<\/strong><\/td>DEL<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001428-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Collie eye anomaly (CEA) <\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>ophthalmic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>from birth<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>NHEJ1<\/td><\/tr>
Mutation<\/strong><\/td>COMPLEX<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000218-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Raine syndrome<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>skeletal<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>FAM20C<\/td><\/tr>
Mutation<\/strong><\/td>G-A<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002015-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

MDR1 gene variant (Ivermectin hypersensitivity)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>metabolic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive; however, carriers with hypersensitivity can also be expected<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>ABCB1<\/td><\/tr>
Mutation<\/strong><\/td>DEL<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001402-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
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