Dr. Hanna Lesicka

Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider in New Hyde Park, New York. Dr. Fernandes is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Acrodermatitis Enteropathica, and CHARGE 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 HNRNPH2-Related Disorder. 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.

Reena Jethva is a Pediatrics provider in Hackensack, New Jersey. Dr. Jethva is rated as an Experienced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Autism Spectrum Disorder, Sunken Fontanelles, HNRNPH2-Related Disorder, and Microcephaly.