General description
includes (15 Euro patent fee for DM Exon2): Degenerative myelopathy (DM exon2)XXL, Leukoencephalomyelopathy (LEMP)XXL, Juvenile laryngeal paralysis & polyneuropathy (JLPP)XXL, Neuroaxonal dystrophy (NAD)XXL, X-linked myopathy (XL-MTM)XXL, Coat length I (long or short hair)XXL
Rottweiler
Order details
| Test number | 8648 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Degenerative myelopathy exon 2 (DM exon 2)
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 |
Juvenile laryngeal paralysis & polyneuropathy (JLPP)
Test specifications
| Symptom complex | neurological |
| Inheritance | autosomal recessive |
| Age of onset | 3 months |
| Causality | causally |
| Gene | RAB3GAP1 |
| Mutation | DEL |
| Literature | OMIA:001970-9615 |
Coat length I + II (long or short hair)
