MOLECULAR SYNDROMOLOGY – Human Genetics and Rare Genetic Syndromes

The focus of this stream is the identification of genetic mutations which may lead to clinically defined syndromes in families/individuals. Once the causative mutation is molecularly identified, it has limitless uses including genetic counseling, in-vitro fertilization programs and healthy lifestyle recommendations.

An integral part of human medicine are KitGen Canada’s preventive programs, which are directly targeted to reveal genetic predispositions to so called civilization disorders, such as cardiovascular diseases, coagulation and metabolic disorders, defects of the immune system and/or neurodegenerative disease.

KitGen Canada’s programs serve as strong preventive tools and are favoured by our clinical patients and providers where lifestyle interest is paramount.