Our health testing levels for the Belgian Malinois
We group breeding programs into three levels based on testing depth. Ask your breeder directly which level they meet.
A breeder at the Great level performs all mandatory tests plus 7 additional clinically recommended screenings that reduce risk in this breed.
In addition to mandatory tests:
Progressive Retinal Atrophy (PRA)(PRA)
Augen
Progressive Retinal Atrophy (PRA) is an inherited eye disease that affects the retina, which is the light-sensitive layer of tissue at the back of the eye. In this condition, the specialized cells responsible for detecting light, known as photoreceptors, gradually degenerate and die. Because these cells cannot recover or be replaced, the disease slowly but inevitably leads to complete blindness.
Retinal Dysplasia(RD)
Augen
Retinal dysplasia is a congenital condition affecting the eyes, where the retina (the light-sensitive tissue at the back of the eye) does not develop properly during growth in the womb. This abnormal development leads to structural defects like folds or gaps in the retinal layers. Because the retina is responsible for sending visual signals to the brain, these imperfections can impair normal vision.
Augen
Juvenile Cardiomyopathy and Mortality (Belgian Malinois)(CJM)
Herz und Kreislauf
Juvenile Cardiomyopathy and Mortality (CJM) is an inherited heart muscle disease caused by a genetic mutation in the YARS2 gene that affects Belgian Shepherd puppies. This condition disrupts the normal structure and function of the heart muscle, preventing it from pumping blood effectively to the rest of the body. Because it is an autosomal recessive disorder, a puppy must inherit the mutated gene from both parents to be affected.
DNA · Passing: Clear or Carrier
Ataxia, CNS atrophy with cerebellar ataxia (Belgian Malinois)(CaCa)
Nervensystem
This is a severe, inherited neurological disorder that causes the progressive breakdown of nerve cells in the brain's coordination center, known as the cerebellum. As these cells degenerate, the dog loses the ability to control and coordinate its voluntary movements. It is an autosomal recessive condition, meaning a puppy must inherit the mutated gene from both parents to develop the disease.
DNA · Passing: CARRIER
Cerebellar Ataxia(CA1)
Nervensystem
Cerebellar Ataxia is an inherited neurological disorder that affects the cerebellum, which is the part of the brain responsible for coordinating movement and balance. Due to an autosomal-recessive genetic mutation, nerve cells in this brain region progressively degenerate. This gradual loss of cells prevents the brain from properly controlling the body's movements.
DNA · Passing: Clear or Carrier
Spongy Degeneration with Cerebellar Ataxia 1 (Belgian Malinois)(SDCA1)
Nervensystem
Spongiöse Degeneration mit zerebellarer Ataxie 1 (SDCA1) is an inherited neurological disease that causes the brain tissue, particularly in the cerebellum, to break down and develop a spongy appearance. The cerebellum is the area of the brain responsible for coordinating voluntary movements and balance. As this tissue degenerates, the dog's nervous system loses the ability to properly control body movements.
DNA · Passing: Clear or Carrier
Spongy Degeneration with Cerebellar Ataxia 2 (Belgian Malinois)(SDCA2)
Nervensystem
Spongiform Degeneration with Cerebellar Ataxia Type 2 (SDCA2) is an inherited neurological disease affecting the brain, specifically the cerebellum, which controls movement and balance. In affected dogs, the brain tissue develops microscopic, sponge-like holes, disrupting the normal transmission of nerve signals. This leads to a severe loss of motor coordination and control.
DNA · Passing: Clear or Carrier
These levels are a comparison framework, not an official certification. They help compare breeding programs at a glance.