$3.5 Million Funds Study Aimed at Applying Precision Medicine to Rare Tumor Disorder

This article, written by Tamara Bhandari, originally appeared in the Washington University School of Medicine News Hub on April 13, 2017. An international leader in neurofibromatosis research has received a $3.5 million grant to study why people with the same genetic mutation – in this case, a mutation that causes the genetic disorder known as […]

Patient Spotlight: Miranda Ehrstein

Miranda Ehrstein was diagnosed with Neurofibromatosis type 1 (NF1) when she was just 18 months old. Now she is an outgoing and enthusiastic 12 year old girl, who loves stuffed animals, Science and swimming, and is determined to never let her NF1 hold her back. Read about Miranda’s journey with NF1, through the eyes of her loving family.