Progressive Retinaatrophie mit Neurodegeneration (PCYT2-Defizienz)
Progressive retinal atrophy with neurodegeneration (PCYT2 deficiency)
General description
A genetic variant of the PCYT2 gene has been found to be associated with a syndromic disease that combines blindness (PRA) and neurodegeneration in the breed Saarloos Wolfhond.
Breeds
Saarloos Wolfhond
Order details
| Test number | 8879 |
| Abbreviation | PCYT2 |
| 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, ophthalmic |
| Inheritance | autosomal recessive |
| Causality | causally |
| Gene | PCYT2 |
| Mutation | A-G |
Detailed description
A genetic variant of the PCYT2 gene has been found to be associated with a syndromic disease that combines blindness and neurodegeneration in the breed Saarloos Wolfhond.\nAffected dogs suffer from early adult-onset retinal degeneration. The ophthalmological findings are consistent with generalized progressive retinal atrophy (PRA), with first clinical signs being observable between 20 and 46 months of age. Moreover, affected dogs show adult-onset neurological deficits including gait abnormalities, hind limb weakness, tremors, ataxia, cognitive decline and behavioral changes, especially aggression towards the owner. Additionally, epileptic seizures were reported in some cases.\nAffected dogs often have to be euthanized because of progression of the neurological signs and impaired quality of life.
