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Genetic Tests
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Genetic testing is done once in a lifetime, it is a unique investment!

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The result obtained is unique to each individual and contributes decisively to the prevention of the development of pathologies and preventive health.

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The personal characteristics evaluated in this genetic test are polygenic traits, i.e., multiple genes contribute to the same characteristic.

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Genetic testing makes it possible to identify:

  • Predisposition for the development of pathologies.

  • Nutritional genetic profile and food intolerances.

  • Genetic profile of athletic performance.

  • Vitamin deficit

  • Common health risks

  • Welfare

  • Predisposition to stress

  • Physical characteristics

  • Features

  • Behavioral

  • Features of

  • Personality

  • Disease Risk

  • Dementia and Mental Health

  • Oncological Risk

  • Planning Risk

  • Family

The tests you can take:

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  • Nutrigenetics

  • Athletic Performance

  • Well-being Genetics

  • Pharmacogenetics Comprehensive Test

  • Allergies

  • Antioxidants

  • Minerals and Vitamins

  • Babytest

  • Bodybuilding

  • Cardiovascular

  • Hair dermo-cosmetics

  • Body dermo-cosmetics

  • Easy dermo-cosmetics

  • Diabetes

  • Endocrinology and metabolism

  • Healthy aging

  • Sports phytotherapy

  •  Gynecology and obstetrics

  •  Facilitated harmonization

  • Inflammation

  • Healthy longevity

  •  Integrative medicine

  •  Microbiome

  • Neurogenerator

  •  Nutrition and weight loss

  •  Functional nutrition

  • Nutrition, quality of life and aesthetics

  • Nutrition

  • Ophthalmology

  • Oncology

  • Organs

  • Pediatrics

  • Relationships

  • Women's health

  •  Men's health

  • Susceptibility to coronavirus

  • 13021

  • Autism spectrum disorder

  • Down's syndrome

  • Other tests

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Most people carry at least one pathogenic mutation in a gene included in our family planning "panel". It usually only becomes a problem if both parents have a pathogenic mutation in one copy of the same gene.

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When this happens, even if neither parent has symptoms, there is a 1 in 4 chance, for each pregnancy, that your child will be affected by the condition associated with the gene.

For more information download the following pdf here:

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