At Children's Minnesota, we focus on research and innovations that make a difference in the care of our patients. From improving day-to-day quality of life for children and teens, to developing new pain management approaches and adopting cutting-edge technologies, our research is completely kid and family-focused.
The genomic medicine program specializes in helping children with complex needs and birth defects on every step of their journey. We help families searching for the causes of their child’s medical problems as well as those who have already received a specific diagnosis and are looking for support and treatment.
We are the only genomic medicine program in Minnesota that focuses exclusively on caring for kids and uses the latest clinical advances in genomics to deliver the best care. We specialize in diagnosis, evaluation and treatment of genetic conditions — from the common to the most complex and rare. In fact, we have a rare disorders clinic for children who do not have a diagnosis for their condition and we help these families get answers.
Andrew Schmidt was the first person in Minnesota to be diagnosed with Pallister-Killian syndrome, an extremely rare genetic disorder that causes cognitive delays.