Dr. Jessica Soni

Punita Gupta is a Pediatrics provider in Paterson, New Jersey. Dr. Gupta is rated as a Distinguished provider by MediFind in the treatment of Triple X Syndrome. Her top areas of expertise are Neurofibromatosis, Neurofibromatosis Type 1 (NF1), Gaucher Disease Type 1, and Gaucher Disease.

Wreida Attia is a Pediatrics provider in New Rochelle, New York. Dr. Attia is rated as an Experienced provider by MediFind in the treatment of Triple X Syndrome. Her top areas of expertise are Triple X Syndrome, Poland Syndrome, Amniotic Band Syndrome, and Multiple Pterygium Syndrome.

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 Triple X Syndrome. His top areas of expertise are Krabbe Disease, Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), and N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3.