Search results for: 'DOG-PRA-PRCD'

This genetic disease is characterized by bilateral deafness in puppies with no other symptoms.

Animals with CSNB show various clinical signs such as night blindness and variable visual deficits. 

Renal cystadenocarcinoma and nodular dermatofibrosis cause kidney tumours, uterine leiomyomas and skin nodules.

Trapped neutrophil syndrome is an immune system disorder. Affected puppies suffer from chronic infections and developmental delays.

Scott syndrome is characterised by an increased tendency to bleed due to altered coagulation activity.

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.

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.