Genetic Test
KIF3B (Kinesin Family Member 3B) is a gene that encodes kinesin proteins responsible for intracellular transport of various substances. Abnormalities in this gene have been associated with retinal degeneration not only in cats but also in humans. This genetic test targets three specific gene variants related to progressive retinal atrophy (PRA).
Disease Description
Progressive retinal atrophy (PRA) is a hereditary disease in cats characterized by gradual degeneration and loss of function of the retina—the light-sensitive tissue located within the eye. Although PRA does not cause pain, it progressively diminishes vision, eventually leading to complete blindness.
