Optimizing Health and Wellness in Fabry Disease with Dr. Staci Kallish скачать в хорошем качестве

Optimizing Health and Wellness in Fabry Disease with Dr. Staci Kallish

This presentation took place on Friday, October 17, 2025 as part of the National Fabry Disease Foundation's 15th Annual Fabry Family Education Conference. Staci Kallish, DO, is an Associate Professor of Clinical Medicine within the Department of Medicine, Division of Translational Medicine and Human Genetics, at Penn Medicine, the Department of Pediatrics at the Children’s Hospital of Philadelphia (CHOP), and the Perelman School of Medicine at the University of Pennsylvania. Dr. Kallish is board-certified in pediatrics, clinical genetics, and clinical biochemical genetics. She completed her pediatric residency training at Cooper University Hospital and her medical genetics fellowship training at CHOP. Dr. Kallish diagnoses and treats both adult and pediatric patients with inherited rare diseases. She has specific interests in lysosomal storage disorders and inherited connective tissue disorders. She also supports clinics for adults with Neurofibromatosis type 1 and sex chromosome disorders. As a pediatrician working in both the pediatric and adult settings, Dr. Kallish is also very interested in the transition of care from pediatric to adult medical settings and in the care of families as a unit. She participates as an investigator in clinical trials for lysosomal storage diseases and other inherited disorders.