Carrying genetic diseases
is important for determining the risk in offspring, since in a “healthy person” carriage of latent mutations can be detected that can manifest themselves in offspring.
Hereditary tumor syndromes and the risks of cancer
is vital for determining a hereditary predisposition to cancer which, when the carriage of a pathogenic polymorphism is detected, makes it possible to develop an individual plan with screening tests to detect the disease early and effectively treat it, as well as to put together recommendations to decrease the risk that the disease will develop further
Multifactorial diseases
- cardiovascular diseases
- endocrine system diseases
- central nervous system diseases
- respiratory system diseases
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musculoskeletal system diseases
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visual organ diseases
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urogenital system diseases
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digestive tract diseases
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skin diseases
Population genetics
analyzes the subject’s origin, where his or her ancestors came from (determining haplogroups). The results are shown on a map of how the haplogroup spread around the world, with the frequency, it is encountered.
Pharmacogenetics
is dedicated to individual sensitivity to medicinal products.
Nutrigenetics
helps determine individual recommendations in terms of diet.
Beauty and Genetics in Fitness
gives recommendations on how to take care of the skin and choose the most effective workout regimen.
