For children with severe bowel diseases Amira holds a PhD in molecular biology and has won several science awards in Algeria. Her research focuses on severe early infantile bowel diseases (VEO-IBD). Her goal is to explore the genetic causes of
Scolar discovers rare gene mutation The biologist from Iran came to Care-for-Rare as a doctoral student with a current case: a brother and sister suffered from a severe bone marrow dysfunction. The cause was unknown, but Ehsan pursued a hunch.