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Hypocatalasia (or acatalasemia) is a rare genetic disorder caused by a mutation in the CAT gene, leading to a severe deficiency of catalase. This enzyme normally protects tissues against oxidative stress. The c.979G>A (p.Ala327Thr) mutation was first identified in a Beagle colony and subsequently detected in pet Beagles. A homozygous dog notably developed oral cavity gangrene with tooth loss at a young age. The disease may remain clinically silent for a long time, which highlights the importance of genetic screening in breeding dogs.
This test is also recommended for the Basset Hound as part of the Flemish government breeding program (see the official program).

The PPARD gene is involved in mechanisms related to energy metabolism, fat utilisation and muscular endurance. In racing pigeons, a recent study suggests that certain variations in this gene may be linked to race performance, particularly return speed and ranking coefficient. The CC genotype for the PPARD c.*271C>T marker is the one that stands out most favourably in the study, notably because it was observed in pigeons taking part in a larger number of races. This test can therefore provide complementary information to guide the selection of breeding birds, without replacing the assessment of the pigeon, its lineage, training and actual racing results.

Cone-rod dystrophy 1 is a form of progressive retinal atrophy characterised by an early, severe and rapidly progressive loss of cone function accompanied by a progressive loss of rods.

Progressive retinal atrophy 1 is one of several forms of progressive retinal atrophy (PRA). The degeneration of the photoreceptors leads to blindness before the age of two.

Stargardt disease 1 is a genetic retinal disorder observed in the Labrador Retriever. It causes progressive degeneration of photoreceptors, initially affecting the visual streak and later the entire retina. Affected dogs show reduced vision, noticeable in both daylight and low-light conditions, with abnormal pupillary reflexes. The progression is slow, and most dogs retain some vision throughout their lives. Heterozygous carriers may show mild retinal abnormalities without obvious visual impairment.

This test is also recommended for the German Shorthaired Pointer as part of the breeding program of the Flemish government (see the official program).

Myotubular myopathy type 1, also known as X-linked myotubular myopathy, is a genetic disease of the skeletal muscles. Clinical signs include hypotonia, muscle atrophy and breathing difficulties. The disease is transmitted in an X-linked recessive manner, so males carrying the mutation will all be affected. However, only females with 2 copies of the mutated allele will be affected.

This pack includes the recommended tests defined by the Flemish breeding program for Caniche miniature: ichthyosis type 1 (DOG-ICHGR-1), Osteochondrodysplasia (DOG-CHONDRO) and Von Willebrand disease type 1 (DOG-VWD1). The Flemish breeding program also makes the tests included in our package mandatory DOG-CANICHE-MINI-VL.

This pack includes the recommended tests defined by the Flemish breeding program for Irish Setter Red and White: Von Willebrand disease type 1 (DOG-VWD1), Canine leukocyte adhesion deficiency type 1 (DOG-CLAD1), Progressive retinal atrophy 1 (DOG-PRA-RCD1) and Degenerative myelopathy 2 (DOG-DM2).

This pack includes the recommended tests defined by the Flemish breeding program for Rhodesian Ridgeback: multifocal retinopathy type 1 (DOG-CMR1), Dystrophic epidermolysis bullosa (DOG-DEB), ichtyosis type 1 (DOG-ICHGR-1) and Neuronal ceroid lipofuscinosis 4A (DOG-NCLA). The Flemish breeding program also makes the tests included in our package mandatory DOG-RR-VL.

Polyneuropathy type 1 (LNP21) is a progressive neuromuscular disease characterised by generalised weakness, hypotonia, laryngeal paralysis and muscle atrophy, particularly of the hind limbs. The age of onset of symptoms can vary between 1 and 11 years.