Services & Specialties
Metabolic Disorders
Newborn Screening, Metabolic Evaluation, Treatment and ResearchOur team at Sanford Children’s Specialty Clinic provides guidance in the evaluation of infants with abnormal newborn screens. Early diagnosis and treatment of many of these diseases help children live normal lives. In addition to providing guidance in evaluating abnormal newborn screens, our team of pediatric geneticist Laura Davis-Keppen, MD, and genetic counselors Quinn Stein, MS, CGC and Amy Woltanski, MS, evaluates and treats individuals with inborn metabolic diseases such as PKU and lysosomal storage diseases. Our team is also involved in innovative research for the treatment of PKU and enzyme replacement therapy for lysosomal storage diseases. Click here to learn more about Dr. Davis-Keppen’s participation in breakthrough research for PKU. To schedule an appointment, please call (605) 333-7188 or 1-800-850-0064. |
