Physician-scientist Anna Greka investigates rare genetic diseases using advanced technology to solve medical mysteries. She explains how her team decodes the secrets of our cells and how this work could help develop precision treatments for millions of people worldwide. Topics discussed include a case study of a family affected by a rare genetic disease, the genetic mutation behind kidney failure, and the link between toxic proteinopathies and various diseases.

Physician-scientist Anna Greka investigates rare genetic diseases, decoding secrets of our cells. Using advanced technology, they solve medical mysteries and develop precision treatments for millions. Insights into human cells, advancements in technology, and uncovering a biological mechanism for treating diseases discussed.

Anna Greka, a physician-scientist dedicated to unraveling rare genetic diseases through advanced technology, sheds light on her groundbreaking research. She discusses the impact of hereditary kidney disease across generations, revealing how a 2013 discovery transformed their understanding. Greka highlights the role of genetic mutations, particularly in the MUC1 gene, in severe health issues. Her work not only aims at pinpointing precise treatments but emphasizes the critical collaboration between scientists and families in solving these medical mysteries.