PREVENTIVE GENETIC TESTS / SENSORS: represent a new step forward in diagnostics in the clinic, with the fundamental goal of implementing personalized medicine in clinical practice. Preventive testing determines the risk of developing the disease, where genetically predisposed people have a higher chance of developing the disease in which the hereditary factor plays an important role.

Preventive genetic tests are performed by swabbing the oral cavity, and depending on the need, about 30 individual tests are available: Gluten Sensor, Lactose Sensor, Pharmaco Sensor, Diabetes Sensor, Hypertension Sensor, Cardiovascular Sensor, Depression Sensor, Thrombo Sensor, Glaucoma Sensor, Sport Sensor, Nutrition Sensor, Weight Sensor…

The crown of all preventive genetic tests is the Premium Plus Sensor, which combines individual preventive tests into a complete picture of the individual with analysis of all organ systems, genetic specifics of detoxification capacities, pharmacological and nutritional characteristics, vitamin and mineral needs, respecting male and female differences.

TEST FOR DETERMINATION OF METABOLIC DISEASES IN CHILDREN (BABY SENSOR 100+): allows testing of more than 110 inherited metabolic disorders. Testing is performed from a urine sample, and due to the possibility of early intervention and timely treatment, the test is intended especially for children up to 5 years of age with symptoms of developmental delay, physical impairment, mental retardation, slow weight gain, convulsions, speech difficulties, specific skin pigmentation…
PATERNITY TEST: is performed by swabbing the oral cavity, where the analysis of 21 internationally recognized loci determines biological parenting with a reliability greater than 99.999%

PRENATAL PATERNITY TESTING: is performed after 10 weeks of pregnancy, from a sample of the mother’s blood and by swabbing the oral cavity of the potential father. Analysis of internationally recognized loci, NGS method, determines biological parenting with the reliability of> 99.9%.

KINSHIP TEST: is performed by swabbing the oral cavity, where based on the analysis of gene loci, it is determined whether the tested persons are blood relatives.

NON-INVASIVE PRENATAL TESTS: These are genetic tests that can be performed from a maternal blood sample after 10 weeks of pregnancy. Due to the presence of fetal cells in the mother’s blood, the existence of chromosomal abnormalities is determined.

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