Our health testing levels for the Parson Russell Terrier
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:
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 or Carrier
Congenital Myasthenic Syndrome(CMS)
Bewegungsapparat
Congenital Myasthenic Syndrome (CMS) is an inherited genetic disorder that disrupts the communication between nerves and muscles. This breakdown in the neuromuscular system prevents signals from reaching the muscles properly, leading to rapid muscle fatigue and weakness. Unlike some other muscle-weakness disorders, this is a congenital condition present from birth and is not caused by an autoimmune system malfunction.
DNA
Ichthyosis(ICT)
Haut und Fell
Ichthyosis is an inherited skin disorder where the outer layer of the skin, the epidermis, does not develop or shed properly. This defect in keratinization—the process of forming a protective outer skin barrier—leads to a buildup of dry, thick, and scaly skin. Because this barrier is compromised, the dog's body is more vulnerable to secondary infections.
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
Globoid cell leukodystrophy (galactocerebrosidosis)(GCL)
Nervensystem
Globoid cell leukodystrophy is an inherited metabolic disorder affecting the nervous system, caused by a deficiency in an essential enzyme. This deficiency leads to the buildup of harmful substances that destroy myelin, which is the protective sheath surrounding nerve fibers in the brain and spinal cord. Without this protective covering, the nerves cannot transmit signals properly, resulting in progressive neurological decline.
DNA
Urolithiasis
Nieren
Urolithiasis is the formation of mineral stones within the urinary tract, which includes the kidneys, bladder, and connecting tubes. These solid crystal clusters develop when minerals in the urine clump together instead of dissolving. Over time, these stones can irritate the sensitive lining of the urinary system or completely block the flow of urine.
These levels are a comparison framework, not an official certification. They help compare breeding programs at a glance.