Katherine L. Nathanson, MD

Dr. Nora Sandorfi, MD, is a Professor of Clinical Medicine in the Division of Rheumatology at the Perelman School of Medicine, University of Pennsylvania, with a special focus on Systemic Sclerosis (scleroderma) and Sjögren’s syndrome. She completed her medical training at Semmelweis University in Budapest, followed by residencies and fellowships in Philadelphia, including at Thomas Jefferson University Hospital. Over the past two decades, Dr. Sandorfi has served as Principal Investigator on numerous clinical trials and mentored rheumatology fellows in the scleroderma specialty clinic. Her commitment to patient education is also notable she regularly participates in outreach and educational events aimed at those living with scleroderma. Dr. Sandorfi is highly regarded for her deep clinical expertise, empathetic communication, and dedication to patient well-being. In her spare time, Dr. Sandorfi is an avid bicyclist.

The Institute for Translational Medicine and Therapeutics (ITMAT) at the University of Pennsylvania is dedicated to advancing research that bridges the gap between basic science and clinical applications, focusing on the development of new and safer medicines. With an extensive network of over 2,500 investigators and partnerships with the Children's Hospital of Philadelphia and other notable institutions, ITMAT supports a comprehensive training platform for both researchers and support staff involved in translational medicine. Since its inception in January 2005, ITMAT has propelled the field of human phenomic science and enhanced collaborative interdisciplinary research through various funding initiatives and educational programs. The institute emphasizes bridging the pediatric to adult healthcare divide and integrates preclinical science with practical drug development, enriching the landscape of translational therapeutics. Generated from the website

As a Clinical Geneticist at Penn Medicine, my goal is to provide diagnostic workup and medical management for any patient with a genetic or inherited condition. With my training in Medical Genetics and Internal Medicine, I see both adult and pediatric patients with any suspected genetic disorder, and have a special interest and expertise in the management of patients with ciliopathy conditions (disease affecting the primary cilium). When visiting our clinic, you can expect a detailed review of your medical and family history, a thorough physical exam, excellent genetic counseling from our team of Genetic Counselors, and a clear and comprehensive plan for diagnostic workup and management.