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O nás: Who We Are
Do you know that....
Approximately 1 in 40 people are carriers of the genetic mutation that causes SMA, making it one of the most common genetic disorders.
In the MENA region, the lack of standardized referral pathways for Duchenne Muscular Dystrophy (DMD) causes delays in diagnosis and treatment. We aim to build AI-driven software to analyze low MRI muscle tissue scan to provide early detection and comprehensive evaluation of disease management.
OUR MAIN PROJECTS INCLUDE:
medical problem solving contest and summer academy focused on clinical practice
journalism for young scientists with a focus on research
weekend workshops
*European Commission, report on Slovakia 2020
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