Through genetic testing, we help doctors to make better informed decisions about diagnosis and prognosis of diseases. This way, they are given the tools to be able to individualize treatment improving patient safety and quality of life.
GENETICS AND DIAGNOSTICS
Common diseases occur at the interface of genes and the environment, as both inherited as well as lifestyle and other health risk factors play important roles in the disease process. A better and more personalized understanding of risk may therefore help to empower individuals and their doctors to implement more rigorous and potentially more effective prevention strategies, with the goal of reducing the likelihood that an inherited predisposition to a given condition may go on to develop into a disease.
Progenika’s core business is the design and production of allele-specific oligonucleotide genotyping microarrays to be used in the diagnosis and prognosis of genetically complex diseases and prediciting response to therapy.
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Familial Hypercholesterolemia
Understanding FH for both you and your family. |
Blood typing
Improving patient safety and blood transfusion compatibility |
Drug response
Improving drug safety and efficacy with a comprehensive test for drug metabolism.
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With the collaboration of:
