The 20 Best N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3 Doctors in The United States

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).

. Dr. Russi 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 125 other conditions, according to our data. His clinical expertise encompasses Increased Head Circumference, Ehlers-Danlos Syndrome (EDS), Chromosome 8p Deletion, and Chromosome 6q Duplication. Dr. Russi is board certified in American Board Of Pediatrics and American Board Of Medical Genetics.

Laura Seth is a primary care provider, practicing in Internal Medicine in Charlotte, North Carolina. She has been practicing medicine for over 34 years. Dr. Seth 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 1 other condition, according to our data. Her clinical expertise encompasses Hypothyroidism, Hyperthyroidism, Maturity Onset Diabetes of the Young, and Peripheral Neuropathy. Dr. Seth is board certified in American Board Of Internal Medicine. Dr. Seth is currently accepting new patients.

Raymond Wang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Wang 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 50 other conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.

Darius Adams is a Medical Genetics provider practicing medicine 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. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Glycogen Storage Disease Type 3, Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). Dr. Adams is board certified in American Board Of Medical Genetics And Genomics. Dr. Adams is currently accepting new patients.

William Wilcox is a Medical Genetics provider practicing medicine in Atlanta, Georgia. He has been practicing medicine for over 38 years. Dr. Wilcox 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 26 other conditions, according to our data. His clinical expertise encompasses Fabry Disease, Achondroplasia, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). Dr. Wilcox is board certified in American Board Of Medical Genetics And Genomics, 1996.

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.

Sara Cathey is a Medical Genetics provider practicing medicine in Charleston, South Carolina. Dr. Cathey 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 10 other conditions, according to our data. Her clinical expertise encompasses Aspartylglucosaminuria, Mucolipidosis Type 4, Fucosidosis, and Sialidosis. Dr. Cathey is currently accepting new patients.

Tamara Kramer is a primary care provider, practicing in Family Medicine in Janesville, Wisconsin. Dr. Kramer is rated as a Distinguished provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), and Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome).

Dr. Gerald Raymond is a clinical geneticist and neurologist at Johns Hopkins where he is also a professor of genetic medicine and neurology. He obtained his MD at the University of Connecticut and was trained in Pediatrics at Johns Hopkins Hospital and Neurology at the Mass. General Hospital. He received additional training in developmental neuropathology at the Universite Catholique de Louvain in Belgium and clinical genetics at the Harvard Program. Dr. Raymond’s research has been at the overlap of genetics and neurology with specific focus on peroxisomal disorders including adrenoleukodystrophy. He has been actively involved in newborn screening for ALD and in developing clinical follow-up programs. He has extensive experience in clinical management of neurogenetic issues including peroxisomal and lysosomal disorders. He presently serves as the Director of the Lysosomal Storage Disease program in the department of Genetic Medicine. Dr. Raymond 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 21 other conditions, according to our data. His clinical expertise encompasses Adrenoleukodystrophy (ALD), Metachromatic Leukodystrophy, Farber Lipogranulomatosis, and CACH Syndrome. Dr. Raymond is board certified in American Board Of Medical Genetics And Genomics and American Board Of Psychiatry And Neurology.

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.

Benjamin Schipper is a primary care provider, practicing in Pediatrics and Internal Medicine in Grandville, Michigan. He has been practicing medicine for over 23 years. Dr. Schipper 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 1 other condition, according to our data. His clinical expertise encompasses Obesity in Children, Food Allergy, Down Syndrome, and Hashimoto Thyroiditis. Dr. Schipper is board certified in American Board Of Pediatrics and American Board Of Internal Medicine.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 8 years. Dr. Priestley 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 21 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics, American Board Of Medical Genetics And Genomics, and American Board Of Pediatrics.

Dr. Julie Hoover-Fong is a Professor of Genetic Medicine and Pediatrics and Director of the Greenberg Center for Skeletal Dysplasias at Johns Hopkins University. Dr. Hoover-Fong holds a bachelor’s degree in Human Nutrition from The Ohio State University, where she also completed her medical degree. She received her Ph.D. in the Graduate Training Program in Clinical Investigation at the Johns Hopkins University School of Medicine and Bloomberg School of Public Health. Dr. Hoover-Fong completed a pediatric internship and residency at Washington University in St. Louis and a fellowship in medical genetics at Johns Hopkins University in Baltimore. She joined the Johns Hopkins University faculty in 2002 and progressed to Professor of Genetic Medicine and Pediatrics in 2019. She practices and oversees the clinical operations, research and educational ventures for the patients, families and healthcare providers served by the Greenberg Center. Her clinical team develops and improves diagnostic and treatment guidelines for comprehensive care of patients with all types of bone conditions including dwarfism, orofacial clefting, craniosynostosis and more. Dr. Hoover-Fong also mentors and teaches medical students, residents and genetic medicine trainees. As an active clinical researcher, Dr. Hoover-Fong is the Principal Investigator of multiple global clinical trials for achondroplasia, the first multi-center, investigator-initiated natural history study for achondroplasia, and multiple clinical studies for patients with orofacial clefting, hypophosphatasia and other conditions. She is also a co-investigator on the ELSI and Phenotype Review Committees for the Mendel Project, a whole exome sequencing venture to identify the genetic cause of Mendelian conditions. From an institutional service perspective, Dr. Hoover-Fong serves on the Johns Hopkins Associate Professor Promotions Committee and the Advisory Committee for the Graduate Training Program in Clinical Investigation. She serves on the Medical Advisory Board of the Little People of America, is a member of the Miller-Coulson Academy of Clinical Excellence at Johns Hopkins University and is a charter member of the International Skeletal Dysplasia Management Consortium, publishing best practice guidelines for patients with skeletal dysplasias. Dr. Hoover 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 26 other conditions, according to our data. Her clinical expertise encompasses Rhizomelic Syndrome, Achondroplasia, Spondyloepimetaphyseal Dysplasia Strudwick Type, Adenoidectomy, and Myringotomy. Dr. Hoover is board certified in American Board Of Medical Genetics And Genomics.

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.

Dr. Michael B. Bober is a pediatric geneticist and an authority on skeletal dysplasias, brittle bone disease, primordial dwarfism and other genetic disorders of the skeleton. He is a frequent guest lecturer, accomplished author and consultant for numerous television networks, here and abroad. Dr. Bober 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 70 other conditions, according to our data. His clinical expertise encompasses Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy. Dr. Bober is board certified in American Board Of Medical Genetics And Genomics.

Sandeep Kapoor is a primary care provider, practicing in Internal Medicine in Studio City, California. Dr. Kapoor 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 3 other conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A), N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, and Mucopolysaccharidoses (MPS).

Luis Umana is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Umana 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 177 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and Argininosuccinic Aciduria.

Richard Chang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chang 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 156 other conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Arginase Deficiency, and Urea Cycle Disorders (UCD). Dr. Chang is currently accepting new patients.

Markey Mcnutt is an Internal Medicine specialist and an Endocrinologist practicing medicine in Dallas, Texas. Dr. Mcnutt 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 122 other conditions, according to our data. His clinical expertise encompasses Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, Phenylketonuria (PKU), and Megalencephalic Leukoencephalopathy with Subcortical Cysts.