Biography:
Hunter Slosser, BS is a medical student at Kansas City University with a strong interest in neuroscience and medical genetics. His research focuses on pharmacogenomics and rare neurological conditions, including Ollier’s disease and its association with astrocytomas. He co-authored a case report highlighting the genetic links between isocitrate dehydrogenase mutations and tumor development. With experience as a Genetic Counselor Assistant and a Teaching Assistant in Neuroscience, Hunter is passionate about advancing precision medicine and understanding the genetic basis of neurological disorders.
Title : Ollier’s disease with grade II astrocytoma case report and brief review of astrocytoma