Our Childhood Epilepsy Panel, co-developed with the Danish Epilepsy Centre in Dianalund, covers 20+ epilepsy-related syndromes and is up to date with the latest genetic research. We can help you achieve a correct diagnosis and lead to the best treatment. Learn more ›
In cases of Progressive Myoclonic Epilepsy, time is critical. However patients of PME are often misdiagnosed or confused with other epilepsy syndromes in the beginning. A correct diagnosis can make a difference in treatment, and our Progressive Myoclonic Epilepsy Panel can help you. Learn more ›
Our Brain Malformations panel covers 25+ syndromes related to brain malformations. We can help you find the diagnosis you are looking for to be able provide the best treatment. Learn more ›
Breast Cancer can be hereditary. Our Panel can reduce the uncertainty over the potential risk of developing Breast Cancer and make an informed decision of your next step. Learn more ›
Colorectal cancer is hereditary in 1 out of 6 cases. Our Hereditary Non-Polyposis Colorectal Cancer panel can help you assess your risk and make an informed decision of your next step.
We cannot change the genes we are born with, but we can study them to know what to expect. We recently helped a family in which little L. had died as a consequence of a SCN8A genetic mutation. There was nothing that could be done about that, but when her mom became pregnant again, knowing that her son did not have the same mutation after a screening was a huge relief for all. With the technology and our experts' knowledge, we have been able to help patients and families in similar situations.