General description
includes (15 Euro patent fee for DM Exon2): Canine multi-focal retinopathy (CMR1), Degenerative myelopathy (exon 2), Dental-skeletal-retinal anomaly (DSRA), Hyperurikosuria (HUU/SLC), Neuronal ceroid lipofuscinosis (NCL)
Italian Cane Corso
Detailed description
The following tests are included in this combination: Canine multi-focal retinopathy (CMR1), Degenerative myelopathy (exon 2), Dental-skeletal-retinal anomaly (DSRA), Hyperurikosuria (HUU/SLC), Neuronal ceroid lipofuscinosis (NCL)
Hyperuricosuria (HUU/SLC)
Order details
| Test number | 8944 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Test specifications
| Symptom complex | urological |
| Inheritance | autosomal recessive |
| Causality | causally |
| Gene | SLC2A9 |
| Mutation | G-T |
| Literature | OMIA:001033-9615 |
Degenerative myelopathy exon 2 (DM exon 2)
Order details
| Test number | 8944 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Test specifications
| Symptom complex | neuromuscular |
| Inheritance | autosomal recessive with age-dependent incomplete penetrance; a risk factor associated with DM is detected. |
| Age of onset | from 8 years |
| Causality | High-risk factor |
| Gene | SOD1 |
| Mutation | G-A |
| Literature | OMIA:000263-9615 |
Canine Multi-Focal Retinopathy CMR1
The symptoms described in this breed can be found in the text above.
Order details
| Test number | 8944 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Test specifications
| Symptom complex | ophthalmic |
| Inheritance | autosomal recessive |
| Age of onset | 4 months |
| Causality | causally |
| Gene | BEST1 |
| Mutation | G-A |
| Literature | OMIA:001444-9615 |
Neuronal Ceroid Lipofuszinosis CLN1
The symptoms described in this breed can be found in the text above.
Order details
| Test number | 8944 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Test specifications
| Symptom complex | neurological |
| Inheritance | autosomal recessive |
| Causality | causally |
| Gene | CTSD |
| Mutation | C-T |
| Literature | OMIA:001504-9615 |
