Search results for: 'DOG-PRA-PRCD'

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.

Familial nephropathy is a kidney disease with progressive destruction of both kidneys. The first symptoms are excessive water consumption, weight loss, reduced appetite and vomiting.

Cerebellar abiotrophy is a neurodegenerative disease. Affected puppies show a variety of symptoms including loss of balance and an asymmetric gait with an inability to regulate speed and amplitude of movement. 

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

Junctional epidermolysis bullosa (JEB) is a recessive genetic disease of the skin and mucous membranes in which the epidermal layer is separated from the skin.

Factor VII deficiency is a genetic disorder affecting blood clotting. Symptoms are related to mild blood clotting disorders such as bleeding and bruising.

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.