Between February 23–March 2, 2026, the Medical Students' Society of Craiova and the Human Genomics Laboratory (LGU - UMFCV), with the support of the University of Medicine and Pharmacy of Craiova, the Cell and Molecular Biology Student Circle, and the Little People’s Association (Asociația Oamenilor Mici), are organizing the third edition of the project 'How to Read the Genetic Code: A Journey into Genetics and Rare Diseases'. This initiative, which has already become an academic tradition, was launched in memory of Professor Mihai Ioana, PhD, a prominent figure in Romanian medical genetics, whose contributions shaped genomic research and education regarding rare diseases.

​The event is part of a series of manifestations dedicated to Rare Disease Day and aims to contribute to the awareness campaign regarding the importance of early diagnosis, advanced research, and community support for individuals affected by complex genetic pathologies. Given that over 70% of rare diseases are genetic in origin, understanding molecular mechanisms represents the foundation of precision medicine for these conditions.

The activities of the project's third edition will debut on February 24, with educational presentations held by UMF Craiova students at the 'Ștefan Velovan' National Pedagogical College, between 12:00 PM and 1:00 PM. On Thursday, February 26, starting at 12:00 PM, the Human Genomics Laboratory (LGU) will open its doors to students, offering them the opportunity to directly discover research activities and the practical applications of genomic medicine in diagnosing rare conditions.

This third edition will conclude with the conference 'A Genetic Puzzle: From Symptoms to Diagnosis in Rare Genetic Diseases,' held on March 2 in the 'Mihai Ioana' Auditorium.  Dedicated to specialists, residents, and students, the conference aims to promote the multidisciplinary approach in the diagnosis and management of rare diseases, as utilized within Centres of Expertise and European Reference Networks (ERNs). Under the symbolic concept of a 'Genetic Puzzle,' the presentations will reconstruct the complex patient journey, from the first clinical manifestations to molecular confirmation and the establishment of therapeutic management.

​Participation in the academic session on March 2, starting at 1:00 PM, is based on registration by completing the form available here

​We look forward to having you join us in this educational initiative. Together, we can transform the challenges of genomic medicine into sustainable opportunities to improve the quality of life for patients with rare diseases.