Familial nephropathy (FN) – English Springer Spaniel, Samoyed
Familial nephropathy (FN)
General description
The Familial or Hereditary Nephropathy (FN) is a juvenile-onset fatal kidney disease. The renal disease caused by FN invariably is progressive and ultimately fatal. Dogs with FN typically develop chronic renal failure between 6 month and 2 years of age, with eventual and sometimes rapid destruction of both kidneys. The first clinical signs are excessive water consumption, growth rate or loss in weight, reduced appetite, and vomiting.
Breeds
English Springer Spaniel, Samoyed
Detailed description
The main functions of the kidneys are to excrete water, foreign substances, electrolytes and metabolic waste products. The glomeruli of the kidney act as a filter, separating urine from blood and thus filtering out the primary urine. A network of Type IV collagen fibres are essential for the correct structure of the glomerular basement membrane and thus for kidney function.
The progressive kidney disease caused by familial or hereditary nephropathy (FN) is caused by a type IV collagen defect. Dogs with FN develop chronic renal dysfunction between the ages of 6 months and 2 years, which eventually, in some cases very rapidly, leads to destruction of both kidneys and death. Initial clinical signs include excessive thirst, reduced growth rate or weight loss, reduced appetite and vomiting.
Familial Nephropathy (FN) - English Springer Spaniel
The symptoms described in this breed can be found in the text above.
Order details
| Test number | 8192 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Test specifications
| Symptom complex | nephrological |
| Inheritance | autosomal recessive |
| Age of onset | 6 months- 2 years |
| Causality | causally |
| Gene | COL4A4 |
| Mutation | G-A |
| Literature | OMIA:002618-9615 |
Familial Nephropathy (FN) - Samoyed
The symptoms described in this breed can be found in the text above.
Order details
| Test number | 8192 |
| Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
| Test duration | 7-14 working days |
Test specifications
| Symptom complex | nephrological |
| Inheritance | X-chromosomal recessive |
| Age of onset | 6 months- 2 years |
| Causality | causally |
| Gene | COL4A5 |
| Mutation | G-T |
| Literature | OMIA:001112-9615 |
