Eva Vanbelleghem

Following my studies in Medicine, I started my training in Clinical Genetics in 2021 and joined the CallewaertLab as a PhD student in 2023. My research focuses on Myhre syndrome, with a particular emphasis on uncovering the profibrotic disease mechanisms associated with this rare genetic disorder. To achieve this, I utilize a combination of zebrafish models, fibroblasts, and organoid systems. This integrative approach enables us to better understand the cellular processes contributing to disease progression, with the ultimate aim of identifying novel therapeutic targets. By combining my clinical training with research, I aim to bridge the gap between basic science and patient care, advancing our knowledge of Myhre syndrome and paving the way for potential treatments.