{"id":218619,"date":"2024-09-12T07:23:53","date_gmt":"2024-09-12T05:23:53","guid":{"rendered":"http:\/\/staging.laboklin.com\/labogen\/labogen_wp\/klubpaket-zwergschnauzer-fellfarbe"},"modified":"2025-07-16T13:25:13","modified_gmt":"2025-07-16T11:25:13","slug":"paket-zwergschnauzer","status":"publish","type":"page","link":"https:\/\/labogen.com\/uk\/pakete-testkombinationen-hund\/paket-zwergschnauzer\/","title":{"rendered":"Paket Zwergschnauzer"},"content":{"rendered":"

Combination Miniature Schnauzer<\/h1>

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

includes: Charcot-Marie-Tooth Neuropathy (CMT), Mycobacterium avium complex sensitivity (MAC), Myotonia congenita, Persistent M\u00fcllerian duct syndrome (PMDS), Progressive retinal atrophy (Type B1-PRA, HIVEP3) and Spondylocostal dysostosis (Comma defect).<\/p>

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

Miniature Schnauzer<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8619<\/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>

Spondylocostal dysostosis (Comma defect)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>skeletal<\/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>HES7<\/td><\/tr>
Mutation<\/strong><\/td>DEL<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001944-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Mycobacterium avium complex sensitivity (MAC)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>immunological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>1-8 months<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>CARD9<\/td><\/tr>
Mutation<\/strong><\/td>DEL<\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Persistent M\u00fcllerian duct syndrome (PMDS)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>urological<\/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>AMHR2<\/td><\/tr>
Mutation<\/strong><\/td>G-A<\/td><\/tr>
Literature<\/strong><\/td>OMIA:002775-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Progressive retinal atrophy (Type B1-PRA, HIVEP3)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>ophthalmic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>HIVEP3<\/td><\/tr>
Mutation<\/strong><\/td>G-A<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001311-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
 <\/div>\n\n\n

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