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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.

Narcolepsy is a genetic disorder caused by a mutation in the orexin receptor. Affected dogs are sleepy and cannot stay awake for long periods. The first signs appear between 4 weeks and 6 months. Narcolepsy is not life-threatening.

Osteogenesis imperfecta, also known as brittle bone disease, is characterised by extreme fragility of bones and teeth caused by an abnormal collagen structure.

Ce profil reprend les analyses spécifiques à effectuer chez le teckel: l'ostéogénèse imparfaite (DOG-OSTEO-T) et la dystrophie des cônes et des bâtonnets (DOG-CRD-SWHD).

This pack includes the recommended tests defined by the Flemish breeding program for Dachshund: Osteogenesis imperfecta (DOG-OSTEO-T), Degenerative myelopathy 2 (DOG-DM2) and Acral Mutilation Syndrome(DOG-AMS). The Flemish breeding program also makes the tests included in our package mandatory DOG-TECK-VL.

This package includes the mandatory tests defined by the Flemish breeding program for Dachshund: Progressive retinal atrophy 4 (CORD1) (DOG-PRA-CRD4), Coat color merle (DOG-LOCUS-M) and Progressive retinal atrophy (NECAP1) (DOG-PRA-NECAP1). The Flemish breeding program also recommends the tests included in our package. DOG-TECK-VL+.

Progressive retinal atrophy is characterised by the relatively early loss of cone photoreceptors while maintaining rod functionality. The first clinical signs appear around the age of 1 to 2 years, progressing to complete blindness.

Acral Mutilation Syndrome is characterised by sensory neuropathy of the paws causing insensitivity to pain in the distal parts. Affected dogs usually show signs of extremity self-mutilation. Proprioception, motor skills and reflexes remain intact.

This test is also recommended for Coton de Tuléar and Teckel as part of the breeding program established by the Flemish government (see official program).

Neuronal ceroid lipofuscinoses (NCLs) are a group of lysosomal storage diseases that affect the central nervous system, leading to early neuronal death and progressive neurodegeneration. NCL2 specifically affects dachshunds, with symptoms including vision loss, tremors, and coordination problems starting at a young age. Unfortunately, there is no known cure for NCL2, and affected dogs typically do not survive past 12 months of age.