Familial hypercholesterolemia is the second most common genetic disease in Sweden, and may have fatal outcomes at a very early age, or reduce life expectancy by 10-15 years in affected individuals.
There are effective treatments already established, but only 18% of the estimated affected people have the diagnosis.
We offer a novel and easy-to-use screening method that performs significantly better than all existing tools today.
Some feedback might have been filtered due to the privacy settings in this hunt.
Outstanding study showing how AI can be used to improve disease diagnosis! In addition, it has many potential applications to other fields and could become an important tool for routine diagnostics in the clinic!
This is a really impactful solution for healthcare and you seem to have a very strong vision and team. Wish you the best of luck!
Reading about this project made me emotional in terms of the positive impact this could make on someone’s life. Thank you and best of luck!!