Neuronale Zeroidlipofuszinose 8 (NCL-8) - Saluki ISAG PRA has been identified in

PRA has been identified in a variety of dog breeds with different inheritance patterns

The dog carries two copies of the dominant D allele and expresses normal undiluted coat colour

Mutation: LAMP3 gene

Primary hyperoxaluria type I (PH I) is an autosomal recessive disorder of glyoxylate metabolism caused by a defective alanine-glyoxylate aminotransferase (AGT) enzyme

Symptoms of the kidney cancer include blood in urine

Neuronale Zeroidlipofuszinose 8 (NCL-8) - Saluki ISAG PRA has been identified inNeuronal ceroid lipofuscinosis (NCLs) are a group of hereditary diseases, characterized by progressive neuronal degeneration and the accumulation of autofluorescent cytoplasmic inclusions in the brain, retina, and other tissues. Clinical symptoms and progress of the disease include increased rates of irritability, with the possibility of outbursts of aggression, hallucinations, hyperactivity and seizures. Most animals lose their ability to coordinate