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Amplexa Genetics A/S

Healthcare Buildings
Medical Devices

What we offer

Amplexa Genetics operates in the field of clinical genetics, developing and implementing clinical genetic tests to help doctors make accurate diagnosis that can make the difference to provide the best treatment. We operate in the fields of neurology, endocrinology, cardiology and oncology. Through skilled researchers, expert advisors and the best technology we are able to offer high quality tests and detailed but easy to read reports, without compromising fast turn around times and competitive pricing.

Products and solutions

Childhood Epilepsy Panel

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 ›

Progressive Myoclonic Epilepsy

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 ›

Brain Malformations

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 Panel

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 (Lynch Syndrome)

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.

Case stories

The Bright side of Genetics - Making Informed Decisions

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.


Niels Christian Ganderup

Amplexa Genetics A/S

Tolderlundsvej 3B, 2
5000 Odense C

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