Lysosomal Disease & Inherited Metabolic Liver Disease Program
Our team of nationally and internationally recognized experts specialize in treating and studying lysosomal storage diseases. These inherited metabolic disorders happen when enzyme deficiencies cause abnormal buildups of toxic materials in the body’s cells. While Gaucher disease is the most common type of lysosomal storage disease, we have deep experience in treating all types of this disease through compassionate, personalized care. We are committed to advancing the science and treatment of Gaucher disease and other lysosomal diseases through state-of-the-art patient care and laboratory research.
Our comprehensive approach is to diagnose and evaluate the burden of disease through a series of tests that help us identify the best treatment path for each patient. Our tests include lab work, MRI and X-ray imaging, echocardiograms, and EKGs.