{"id":228716,"date":"2024-09-12T07:23:54","date_gmt":"2024-09-12T05:23:54","guid":{"rendered":"http:\/\/staging.laboklin.com\/labogen\/labogen_wp\/paket-heilige-birma"},"modified":"2024-09-12T07:23:54","modified_gmt":"2024-09-12T05:23:54","slug":"paket-heilige-birma","status":"publish","type":"page","link":"https:\/\/labogen.com\/en\/pakete-testkombinationen-katze\/paket-heilige-birma\/","title":{"rendered":"Paket Heilige Birma"},"content":{"rendered":"

Combination Birman<\/h1>

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

includes: genetic blood group, Hypotrichosis, Mucopolysaccharidosis type VI (MPS6), polycystic kidney disease (PKD) and progressive retinal atrophy (pd-PRA)<\/p>

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

Birman (Sacred cat of Burma)<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8716<\/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>

Progressive retinal atrophy (pd-PRA)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>ophthalmic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>5 weeks <\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>AIPL1<\/td><\/tr>
Mutation<\/strong><\/td>C-T<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001222-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Hypotrichosis and short life expectancy<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>systemic<\/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>FOXN1<\/td><\/tr>
Mutation<\/strong><\/td>DEL<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001949-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Polycystic kidney disease (PKD)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>nephrological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal dominant<\/td><\/tr>
Age of onset<\/strong><\/td>8 months<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>PKD1<\/td><\/tr>
Mutation<\/strong><\/td>C-A<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000807-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Mucopolysaccharidosis type VI (MPS6)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>systemic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>ARSB<\/td><\/tr>
Mutation<\/strong><\/td>A-G, C-T<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000666-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Genetic blood group <\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>hematologic<\/td><\/tr>
Inheritance<\/strong><\/td>Allelische Reihe nach Dominanz: N>c>b<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Gene<\/strong><\/td>CMAH<\/td><\/tr>
Mutation<\/strong><\/td>COMPLEX<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000119-9685<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
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