Dr. Jaya B. Ganesh

Dr. Marion is Executive Director of the Children’s Evaluation and Rehabilitation Center and the University Center of Excellence in Developmental Disabilities at the Rose F. Kennedy Center. He is Chief of the Divisions of Genetics and of Development Medicine at the Children’s Hospital at Montefiore and Director of the Center for Congenital Disorders. A faculty member at Einstein since 1984, Dr. Marion’s interests include the natural history and genetic basis of multiple malformation syndromes. At The Children’s Hospital at Montefiore he has served as Medical Director of the Spina Bifida Center for 20 years, is the founder and Medical Director of the Williams Syndrome Center, and helped organize the Center for CardioG enetics, the Neurofibromatosis Center, and the Center for Excellence in Autism. He has published extensively in the medical literature in these areas and, in addition, is the author of seven books. Dr. Marion is rated as an Advanced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. His top areas of expertise are Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, and Mucopolysaccharidoses (MPS).

Darius Adams is a Medical Genetics provider in Morristown, New Jersey. Dr. Adams is rated as an Advanced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. His top areas of expertise are Phenylketonuria (PKU), Glycogen Storage Disease Type 3, Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), and Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome). Dr. Adams is currently accepting new patients.

Paul Levy, MD, is Director, Center for Inherited Metabolic Disorders and Director, Inherited Metabolic Disease Specialty Care Referral Center at the Children’s Hospital at Montefiore Einstein. He is also Associate Professor, Pediatrics and Pathology at our Albert Einstein College of Medicine. Dr. Levy sees patients with complex medical issues that may have a genetic etiology. He has a special interest in inherited metabolic disorders, including phenylketonuria (PKU), lysosomal storage diseases and urea cycle disorders, and sees newborns referred by the New York State Newborn Screening Program with positive screens. Dr. Levy is rated as an Advanced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. His top areas of expertise are Krabbe Disease, Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), and N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3.