Our health testing levels for the Epagneul Breton
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 11 additional clinically recommended screenings that reduce risk in this breed.
In addition to mandatory tests:
Cleft palate
Allgemeine Fitness und Anatomie
A cleft palate is a congenital birth defect where the roof of the mouth fails to fuse properly during development in the womb. This failure leaves an abnormal opening between the oral cavity and the nasal passages. Because these two systems are directly connected, food, liquids, and air cannot be properly separated during swallowing.
Physisch · Passing: CLEAR
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.
Passing: CARRIER
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 · Passing: CLEAR
Primary Open-Angle Glaucoma(POAG)
Augen und Sehvermögen
Primary open-angle glaucoma is an inherited eye disease where the natural fluid inside the eye cannot drain properly. This fluid buildup causes a gradual increase in pressure within the eyeball, which eventually damages the optic nerve, the connection between the eye and the brain. Without management, this pressure leads to permanent blindness.
Augen · Passing: CLEAR
Lens luxation(PLL)
Augen und Sehvermögen
Lens luxation is an inherited eye disorder where the lens slips out of its normal position because the supporting fibers holding it in place weaken or break. When the lens shifts, it can block the natural drainage of fluid within the eye. This blockage causes a rapid, painful buildup of pressure called glaucoma, which can lead to permanent blindness if left untreated.
Augen · Passing: CLEAR
Ventricular septal defect(VSD)
Herz
A ventricular septal defect (VSD) is a congenital heart defect where a hole exists in the wall, or septum, that separates the left and right lower chambers of the heart. This opening allows blood to flow abnormally between these chambers, forcing the heart and lungs to work much harder than normal. Over time, this abnormal circulation can lead to fluid accumulation in the lungs and heart failure.
Passing: NORMAL
Complement deficiency(C3D)
Immunsystem
This is an inherited disorder of the immune system where the dog lacks key proteins belonging to the complement system. The complement system is a group of proteins in the blood that normally work together to help the body recognize and destroy invading bacteria. Without these proteins, the dog's natural defense mechanism is severely compromised.
DNA · Passing: CARRIER
Cerebellar abiotrophy(CA)
Nervensystem
Cerebellar abiotrophy is an inherited neurological disorder affecting the brain, specifically the cerebellum, which regulates balance and movement coordination. In affected dogs, the nerve cells in this region prematurely degenerate and die off. This progressive cell loss disrupts the brain's ability to control smooth physical movements.
DNA · Passing: CARRIER
Epilepsy(IE)
Nervensystem
Epilepsy is a chronic disorder of the brain and nervous system where abnormal electrical activity causes sudden, temporary disruptions in normal brain function. These disruptions lead to repeated seizures, which are involuntary changes in body movement, sensation, or behavior. Because the underlying cause is often complex, the brain's electrical signaling remains permanently prone to these sudden misfires.
Physisch
Spinal muscular atrophy(SMA)
Nervensystem
Spinal muscular atrophy is an inherited neurological disorder that affects the motor neurons, which are the specialized nerve cells in the spinal cord that control voluntary muscle movement. Because of an inherited genetic defect, these nerve cells progressively waste away, preventing normal signals from reaching the muscles. This lack of stimulation leads to severe muscle weakness and wasting, known as atrophy, throughout the body.
DNA · Passing: CARRIER
Primary hypothyroidism
Stoffwechsel
Primary hypothyroidism is an endocrine disorder where the thyroid gland, located in the neck, fails to produce enough thyroid hormones. This hormone deficiency is usually caused by the immune system mistakenly attacking the gland or by the gradual replacement of thyroid tissue with fat. Because these hormones regulate how the body uses energy, a shortage slows down the dog's entire metabolism.
Passing: Normal
These levels are a comparison framework, not an official certification. They help compare breeding programs at a glance.