{"id":274856,"date":"2024-09-12T07:24:01","date_gmt":"2024-09-12T05:24:01","guid":{"rendered":"https:\/\/staging.laboklin.com\/labogen\/labogen_wp\/index.php\/pacchetti-combinazioni-di-test-cane\/combination-lagotto-romagnolo\/"},"modified":"2024-09-12T07:24:01","modified_gmt":"2024-09-12T05:24:01","slug":"combination-lagotto-romagnolo","status":"publish","type":"page","link":"https:\/\/labogen.com\/it\/pacchetti-combinazioni-di-test-cane\/combination-lagotto-romagnolo\/","title":{"rendered":"Combination Lagotto Romagnolo"},"content":{"rendered":"

Combination Lagotto Romagnolo<\/h1>

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

includes: Juvenile epilepsy (JE), Lagotto storage disease (LSD), Progressive retinal atrophy (prcd-PRA) and Furnishing (wire hair)<\/p>

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

Lagotto Romagnolo<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8499<\/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>

Furnishing (wire hair)<\/h4><\/div>
Test specifications<\/summary>
Inheritance<\/strong><\/td>autosomal dominant<\/td><\/tr>
Gene<\/strong><\/td>RSPO2<\/td><\/tr>
Mutation<\/strong><\/td>COMPLEX<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001531-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Lagotto storage disease (LSD)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive with incomplete penetrance<\/td><\/tr>
Age of onset<\/strong><\/td>4 months - 4 years <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>ATG4D<\/td><\/tr>
Mutation<\/strong><\/td>C-T<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001954-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Juvenile epilepsy (JE)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>5-12 weeks<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>LGI2<\/td><\/tr>
Mutation<\/strong><\/td>A-T<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001596-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Progressive retinal atrophy (prcd-PRA)<\/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>PRCD<\/td><\/tr>
Mutation<\/strong><\/td>C-T<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001298-9615<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
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