{"id":274601,"date":"2024-09-12T07:24:01","date_gmt":"2024-09-12T05:24:01","guid":{"rendered":""},"modified":"2024-09-12T07:24:01","modified_gmt":"2024-09-12T05:24:01","slug":"combination-belgischer-hollaendischer-schaeferhund","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-belgischer-hollaendischer-schaeferhund\/","title":{"rendered":"Combination Belgischer\/Holl\u00e4ndischer Sch\u00e4ferhund"},"content":{"rendered":"

Combination Belgischer\/Holl\u00e4ndischer Sch\u00e4ferhund<\/h1>

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

includes (15 Euro patent fee for DM Exon2): Cardiomyopathy with juvenile mortality (CJM), CNS atrophy with cerebellar ataxia (CACA), Degenerative myelopathy (DM exon 2), Spongy degeneration with cerebellar ataxia type 1 and 2 (SDCA1 and SDCA2)<\/p>

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

Belgian Shepherd Dog, Dutch Shepherd Dog, Groenendael, Laekenois, Malinois, Tervueren<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8634<\/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>

Spongy degeneration with cerebellar ataxia type 2 (SDCA2)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>5-8 weeks <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>ATP1B2<\/td><\/tr>
Mutation<\/strong><\/td>COMPLEX<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002110-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Spongy degeneration with cerebellar ataxia type 1 (SDCA1)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>5-8 weeks <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>KCNJ10<\/td><\/tr>
Mutation<\/strong><\/td>T-C<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002089-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

CNS atrophy with cerebellar ataxia (CACA)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neuromuscular<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>2 weeks <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>SELENOP<\/td><\/tr>
Mutation<\/strong><\/td>COMPLEX<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002367-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Cardiomyopathy with juvenile mortality (CJM)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>cardiologisch<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>6-8 weeks <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>YARS2<\/td><\/tr>
Mutation<\/strong><\/td>G-A<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002256-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
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