{"id":238372,"date":"2024-09-12T07:23:54","date_gmt":"2024-09-12T05:23:54","guid":{"rendered":"http:\/\/staging.laboklin.com\/labogen\/labogen_wp\/paket-quarab"},"modified":"2024-09-12T07:23:54","modified_gmt":"2024-09-12T05:23:54","slug":"paket-quarab","status":"publish","type":"page","link":"https:\/\/labogen.com\/uk\/pakete-testkombinationen-pferd\/paket-quarab\/","title":{"rendered":"Paket Quarab"},"content":{"rendered":"

Combination Quarab<\/h1>

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

includes: PSSM, HERDA, GBED, CA and SCID<\/p>

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

Arabian Horse, Quarab, Quarter Horse<\/p><\/div>

Order details<\/summary>
Test number<\/strong><\/span><\/td>8372<\/td><\/tr>
Sample material<\/strong><\/td>0.5 ml EDTA blood, mane\/tail hair roots<\/td><\/tr>
Test duration<\/strong><\/td>7-14 working days<\/td><\/tr><\/table><\/details><\/div>
Order now ...<\/a><\/strong><\/div><\/div><\/div>
<\/div><\/div>

Glycogen branching enzyme deficiency (GBED)<\/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>
Literature<\/strong><\/td>OMIA:000420-9796<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Polysaccharid storage myopathy type 1 (PSSM)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>muscular<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal dominant<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Literature<\/strong><\/td>OMIA:001158-9796<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Hereditary eqine regional dermal asthenia (HERDA)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>dermatologic<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000327-9796<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Cerebellar abiotrophy (CA)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>neurological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>6 weeks - 4 months<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000175-9796<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>

Severe combined immunodeficiency (SCID)<\/h4><\/div>
Test specifications<\/summary>
Symptom complex<\/strong><\/td>immunological<\/td><\/tr>
Inheritance<\/strong><\/td>autosomal recessive<\/td><\/tr>
Age of onset<\/strong><\/td>10 days -2 months<\/td><\/tr>
Causality<\/strong><\/td>causally<\/td><\/tr>
Literature<\/strong><\/td>OMIA:000220-9796<\/a><\/td><\/tr><\/table><\/details><\/div><\/div><\/div>
<\/div><\/div>
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