The 20 Best N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3 Doctors Near Me in New York, US

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 a Distinguished provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 6 other conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, and Mucopolysaccharidoses (MPS).

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. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses 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.

Dr. Jan is the Division Director of General Pediatrics where she oversees clinical, teaching, and research operations for the Division of General Pediatrics for Cohen Children's Medical Center. She is also the Medical Director of the Health Homes Serving Children Program for Northwell Health, a care management program for pediatric Medicaid beneficiaries with complex medical or behavioral health needs. Dr. Jan has over a decade of clinical, programmatic and research experience in general pediatrics and general internal medicine. She specializes in the care of children and adults with complex medical needs and intellectual/developmental disabilities. She is the principal investigator of several federally and foundation funded research projects focusing on the delivery of healthcare and long-term care services for children and adults with chronic conditions originating in childhood. Dr. Jan earned her bachelor's degree from the City University of New York at Brooklyn College and her medical degree from the State University of New York Downstate Medical Center. She completed a dual residency in both pediatrics and internal medicine from the University of Pittsburgh Medical Center where she was also Chief Resident. She continued her fellowship training as a Robert Wood Johnson Foundation Clinical Scholar at the Perelman School of Medicine at UPenn, earning a master's in health policy research. Dr. Jan is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses COVID-19, Sickle Cell Disease, Hemoglobinopathy, and Congenital Hemolytic Anemia. Dr. Jan is board certified in American Board Of Pediatrics and American Board Of Internal Medicine.

Jessica Gold is a Medical Genetics provider practicing medicine in Great Neck, New York. Dr. Gold is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. Her clinical expertise encompasses Arachnodactyly, Achard Syndrome, Gaucher Disease Type 3, and Gaucher Disease Type 1.

Jaya Ganesh is a Pediatrics provider practicing medicine in New York, New York. Dr. Ganesh is rated as an Advanced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 64 other conditions, according to our data. Her clinical expertise encompasses Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Danon Disease.

Ricky Hsu is a primary care provider, practicing in Internal Medicine in New York, New York. Dr. Hsu is rated as an Advanced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses HIV/AIDS, Myelitis, AIDS Dementia Complex, and AIDS Dysmorphic Syndrome.

Alejandro Iglesias, MD is Assistant Professor of Pediatrics, Director of the Inherited Metabolic Program, Program Director of the Medical Genetics Residency program and Attending Physician in the Division of Medical Genetics, Department of Pediatrics at New York Presbyterian Hospital/Columbia University Medical Center. He is a clinical and biochemical geneticist primarily interested in inherited metabolic disorders and neurogenetics and dysmorphology. In his role as Director of the Inherited Metabolic Program he is deeply involved in all aspects related with the diagnosis, management and overall care of patients and families with these disorders. In addition, he is in charge of the education of young physicians and medical students in the field of IMD. As an educator, he is in charge of the medical biochemistry lecture series for the first year medical students at the Physicians & Surgeons Medical School at Columbia University paving the way for a new generations of brilliant medical students at Columbia University. Finally, his involvement with the diagnosis and care of patients with X-linked adrenoleukodystrophy has been one of his main accomplishments in the recent years, especially since the introduction of newborn screening in New York State. He has a been involved from the beginning in the development of the program and is active member of the NYS group of metabolic physicians taking care of these patients. In addtion he has been actively involved in all developments asscoiated with newborn screening for Krabbe disease and Pompe disease. Dr. Iglesias is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Hypotonia, Microcephaly, Achalasia Microcephaly Syndrome, and Cortical Dysplasia. Dr. Iglesias is board certified in Pediatrics, Clinical Genetics And Genomics (MD), and Clinical Biochemical Genetics. Dr. Iglesias is currently accepting new patients.

Gustavo Maegawa is a Medical Genetics provider practicing medicine in New York, New York. Dr. Maegawa is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Krabbe Disease, Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, and Gaucher Disease. Dr. Maegawa is board certified in Clinical Genetics And Genomics (MD) and Medical Biochemical Genetics. Dr. Maegawa is currently accepting new patients.

Taryn Draxler is a primary care provider, practicing in Internal Medicine in Penn Yan, New York. Dr. Draxler is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Dementia, Neuronal Intranuclear Inclusion Disease (NIID), Mcleod Neuroacanthocytosis Syndrome, and Huntington Disease.

Prashanth Mannam is a primary care provider, practicing in Internal Medicine in Bronx, New York. Dr. Mannam is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses High Cholesterol, Xanthoma, Familial Combined Hyperlipidemia, and Cirrhosis.

Carlos Mares-Beltran is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Albany, New York. Dr. Mares-Beltran is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Mucolipidosis 3, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Tetrasomy 9p.

Murray Werzberger is a primary care provider, practicing in Internal Medicine in Brooklyn, New York. Dr. Werzberger is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 28 other conditions, according to our data. His clinical expertise encompasses Erectile Dysfunction (ED), Persistent Genital Arousal Disorder, Sitosterolemia, and Ethmoiditis.

Betty Parisis is a primary care provider, practicing in Family Medicine in Lynbrook, New York. Dr. Parisis is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 16 other conditions, according to our data. Her clinical expertise encompasses Glossitis, Pernicious Anemia, Familial Combined Hyperlipidemia, and Xanthoma.

Tun Lin is a primary care provider, practicing in Internal Medicine in Elmhurst, New York. Dr. Lin is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 26 other conditions, according to our data. His clinical expertise encompasses Sitosterolemia, Hyperlipoproteinemia Type 5, Familial Lipoprotein Lipase Deficiency, and Apolipoprotein C2 Deficiency.

Mathew Kladney is a primary care provider, practicing in Internal Medicine in New York, New York. Dr. Kladney is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. His clinical expertise encompasses N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, Mucopolysaccharidoses (MPS), and Musculocontractural Ehlers-Danlos Syndrome (mcEDS).

Ming Cheung is a primary care provider, practicing in Internal Medicine in Flushing, New York. Dr. Cheung is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Eschar, Cellulitis, Peptic Ulcer, and Necrosis.