{"id":274643,"date":"2024-09-12T07:24:01","date_gmt":"2024-09-12T05:24:01","guid":{"rendered":"https:\/\/staging.laboklin.com\/labogen\/labogen_wp\/index.php\/%d0%bf%d0%b0%d0%ba%d0%b5%d1%82%d0%b8-%d0%ba%d0%be%d0%bc%d0%b1%d1%96%d0%bd%d0%b0%d1%86%d1%96%d1%97-%d1%82%d0%b5%d1%81%d1%82%d1%96%d0%b2-%d1%81%d0%be%d0%b1%d0%b0%d0%ba%d0%b0\/combination-bullterrier\/"},"modified":"2024-09-12T07:24:01","modified_gmt":"2024-09-12T05:24:01","slug":"combination-bullterrier","status":"publish","type":"page","link":"https:\/\/labogen.com\/uk\/%d0%bf%d0%b0%d0%ba%d0%b5%d1%82%d0%b8-%d0%ba%d0%be%d0%bc%d0%b1%d1%96%d0%bd%d0%b0%d1%86%d1%96%d1%97-%d1%82%d0%b5%d1%81%d1%82%d1%96%d0%b2-%d1%81%d0%be%d0%b1%d0%b0%d0%ba%d0%b0\/combination-bullterrier\/","title":{"rendered":"Combination Bullterrier"},"content":{"rendered":"

Combination Bullterrier<\/h1>

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

includes: Laryngeal paralysis (LP), Lethal acrodermatitis (LAD) and Primary lens luxation (PLL))<\/p>

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

Bull Terrier, Miniature Bull Terrier<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8474<\/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>

Primary lens luxation (PLL)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>ophthalmic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive; the literature describes that 2-20% of PLL carriers (N\/PLL) develop PLL in the course of their lives. Carriers therefore have an (albeit low) risk of developing PLL.<\/td><\/tr>
Age of onset<\/strong><\/td>3-8 years <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>ADAMTS17<\/td><\/tr>
Mutation<\/strong><\/td>G-A<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000588-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Lethal acrodermatitis (LAD)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>dermatologic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>first week of life <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>MKLN1<\/td><\/tr>
Mutation<\/strong><\/td>T-G<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002146-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Laryngeal paralysis (LP)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive with incomplete penetrance<\/td><\/tr>
Causality<\/strong><\/td>High-risk factor<\/td><\/tr>
Gene<\/strong><\/td>RAPGEF6<\/td><\/tr>
Mutation<\/strong><\/td>INS<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002222-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
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