Search results for: 'DOG-PRA-PRCD'

Leukoencephalomyelopathy is a neurodegenerative disease characterised by a progressive loss of mobility and coordination of the limbs. The first symptoms usually appear between 1 and 4 years of age.

Copper toxicosis is characterised by an accumulation of copper in the liver and other organs leading to chronic hepatitis and cirrhosis of the liver which may progress to necrosis.

Gangliosidosis is a genetic defect that causes the storage of GM1 gangliosides in various tissues. The clinical signs of the disease are progressive neurological dysfunction and growth retardation

Osteogenesis imperfecta, also known as brittle bone disease, is characterised by extreme fragility of bones and teeth caused by an abnormal collagen structure.

Leukoencephalomyelopathy (LEMP) is a neurodegenerative disease characterised by a progressive loss of mobility and coordination of the limbs. The first symptoms usually appear between 1 and 3 years of age.

Neuroaxonal dystrophy is a genetic neurodegenerative disease. Symptoms include various neurological symptoms such as abnormal gait, loss of balance, head tremors and involuntary eye movements (nystagmus).

Inflammatory pulmonary disease is a genetic disease affecting the immune system. Symptoms include fever, cough, difficulty breathing and foamy vomiting. The first clinical signs appear at birth.

Von Willebrand disease is a condition that causes excessive bleeding due to a lack or reduced level of von Willebrand factor (vWF), a blood clotting protein. 

Juvenile myoclonic epilepsy is a genetic defect that causes myoclonic jerks described as electric shocks. Seizures occur daily in over 85% of cases.

Gangliosidosis is a genetic defect that causes the storage of GM1 gangliosides in various tissues. The clinical signs of the disease are progressive neurological dysfunction and growth retardation