Our health testing levels for the Continental Toy Spaniel (Papillon)
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 6 additional clinically recommended screenings that reduce risk in this breed.
In addition to mandatory tests:
Progressive Retinal Atrophy (PRA), CNGB1-related(PRA-CNGB1)
Augen
This is an inherited eye disease where a genetic mutation in the CNGB1 gene causes the light-sensitive cells of the retina at the back of the eye to slowly degenerate. Over time, these photoreceptor cells, which are responsible for capturing light and sending visual signals to the brain, stop functioning and die off. This leads to a progressive and permanent loss of vision in both eyes.
Passing: Clear or Carrier
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: frei / CLEAR
Cataract(HC)
Augen und Sehvermögen
A cataract is a progressive clouding of the lens inside the dog's eye, which is the clear structure that focuses light onto the retina at the back of the eye. When the lens becomes cloudy or opaque, it blocks light from entering, gradually impairing the dog's vision. If left untreated, this condition can eventually lead to complete blindness in the affected eye.
Augen · Passing: CLEAR
Color Dilution Alopecia (CDA)(CDA)
Haut und Fell
Color Dilution Alopecia is a genetic skin disorder that affects dogs with diluted coat colors, such as blue, fawn, or lilac. It is caused by an abnormal distribution of pigment within the hair shafts, which makes the hair brittle and prone to breaking. This structural weakness leads to progressive hair loss and leaves the skin more vulnerable to irritation.
Haut · Passing: Clear or Carrier
Mitral valve dysplasia(MVD)
Herz
Mitral valve dysplasia is a congenital heart defect where the mitral valve, which acts as a one-way gate on the left side of the heart, does not form correctly. This malformation prevents the valve from closing tightly, allowing blood to leak backward instead of pumping efficiently to the body. Over time, this leakage strains the heart muscle, which can lead to heart enlargement and eventual heart failure.
Ultraschall · Passing: NORMAL
von Willebrand's disease(vWD)
Stoffwechsel
Von Willebrand disease is an inherited bleeding disorder that affects the blood's ability to clot properly. It is caused by a deficiency or malfunction of the von Willebrand factor, a specific protein that helps blood platelets stick together to plug damaged blood vessels. Without enough of this functional protein, the clotting process is delayed, which can lead to excessive bleeding even from minor injuries.
Passing: Clear or Carrier
These levels are a comparison framework, not an official certification. They help compare breeding programs at a glance.