General description
includes (15 Euro patent fee for DM Exon2): Degenerative myelopathy (DM exon 2), Neonatal encephalopathy with seizures (NEWS), Progressive retinal atrophy*** (prcd-PRA), Progressive retinal atrophy(rcd4-PRA), von-Willebrand disease type I (vWD 1)
Labradoodle, Miniature Poodle, Poodle, Toy Poodle
Order details
| Test number | 8621 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Neonatal encephalopathy with seizures (NEWS)
Test specifications
| Symptom complex | neurological |
| Age of onset | from birth |
| Causality | causally |
| Gene | ATF2 |
| Mutation | A-C |
| Literature | OMIA:001471-9615 |
Degenerative myelopathy exon 2 (DM exon 2)
Test specifications
| Symptom complex | neuromuscular |
| Age of onset | ab 8 years |
| Causality | High-risk factor |
| Gene | SOD1 |
| Mutation | G-A |
| Literature | OMIA:000263-9615 |
Progressive retinal atrophy (rcd4-PRA)
Test specifications
| Symptom complex | ophthalmic |
| Age of onset | 5-12 years |
| Causality | causally |
| Gene | PCARE |
| Mutation | INS |
| Literature | OMIA:001575-9615 |
von-Willebrand disease type I (vWD1)
Test specifications
| Symptom complex | hematologic |
| Causality | causally |
| Gene | VWF |
| Mutation | G-A |
| Literature | OMIA:001057-9615 |
Progressive retinal atrophy (prcd-PRA)
Test specifications
| Symptom complex | ophthalmic |
| Causality | causally |
| Gene | PRCD |
| Mutation | C-T |
| Literature | OMIA:001298-9615 |
