On this episode, we will chat with Andrew about his daughter and her diagnosis with Pfeiffer Syndrome. Pfeiffer Syndrome is a rare genetic disorder characterized by premature fusion of cranial bones. There are also abnormalities of the limbs and face. According to Seattle Childrens hospital, 1 in 100000 newborns can have this syndrome. Pfeiffer Syndrome is caused by the mutation of FGFR1 and FGFR2 gene. We will chat with Andrew about their journey with Pfeiffer Syndrome on this episode of, What has changed your life?
