The 20 Best Multiple Sulfatase Deficiency Doctors in New York, US

Dr. Yael Zack is a member of White Plains Hospital Physician Associates, Oncology & Hematology of White Plains. Dr. Zack is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Anemia, Paget Disease of the Breast, Large-Cell Immunoblastic Lymphoma, and Familial Colorectal Cancer.

Manisha Balwani is a Medical Genetics provider in New York, New York. Dr. Balwani is rated as a Distinguished provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, Gaucher Disease Type 1, and Gaucher Disease Type 2.

Jaya Ganesh is a Pediatrics provider in New York, New York. Dr. Ganesh is rated as a Distinguished provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Danon Disease.

David Tegay is a Medical Genetics provider in Great Neck, New York. Dr. Tegay is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are KBG Syndrome, Gaucher Disease, Gaucher Disease Type 2, and Gaucher Disease Type 3.

Jessica Gold is a Medical Genetics provider in Great Neck, New York. Dr. Gold is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Maple Syrup Urine Disease, Arachnodactyly, Achard Syndrome, and Ornithine Transcarbamylase Deficiency.

Mark Zambron is a primary care provider, practicing in Internal Medicine in Buffalo, New York. Dr. Zambron is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Anton Syndrome.

Martin Bialer is a Medical Genetics specialist and a Pediatrics provider in Manhasset, New York. Dr. Bialer is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Gaucher Disease Type 3, Gaucher Disease, Gaucher Disease Type 1, and Gaucher Disease Type 2.

Tonia Kim is an Internal Medicine provider in New York, New York. Dr. Kim is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Acute Kidney Failure, Chronic Kidney Disease, Fabry Disease, and End-Stage Renal Disease (ESRD).

Olusegun Ogunfowora is a primary care provider, practicing in Internal Medicine in Far Rockaway, New York. Dr. Ogunfowora is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Hypertension, Familial Hypertension, Glucocorticoid-Remediable Aldosteronism, Gastrostomy, and Ureteroscopy.

Berrin Monteleone is a Pediatrics provider in Garden City, New York. Dr. Monteleone is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are 1p36 Deletion Syndrome, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Gaucher Disease.

Carlos Mares-Beltran is a Medical Genetics specialist and a Pediatrics provider in Albany, New York. Dr. Mares-Beltran is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Mucolipidosis 3, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Chromosome 6 Uniparental Disomy.

Joan Pellegrino is a Medical Genetics specialist and a Pediatrics provider in Syracuse, New York. Dr. Pellegrino is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Krabbe Disease, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.

Anju Ohri is a Hematologist in New Hyde Park, New York. Dr. Ohri is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Multiple Myeloma, Thrombocytopenia, Childhood Iron Deficiency Anemia, and Iron Deficiency Anemia.

Ayuko Iverson is a Medical Genetics provider in New York, New York. Dr. Iverson is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are BRCA Positive Breast Cancer, Li-Fraumeni Syndrome, HER2 Negative Breast Cancer, and Chromosome 9p Deletion.

David Kronn is a Medical Genetics specialist and a Pediatrics provider in Hawthorne, New York. Dr. Kronn is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Pompe Disease, Phenylketonuria (PKU), Krabbe Disease, and Gaucher Disease.

Gustavo Maegawa is a Medical Genetics provider in New York, New York. Dr. Maegawa is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Krabbe Disease, Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, and Gaucher Disease. Dr. Maegawa is currently accepting new patients.

Deirdre Sawinski is a Nephrologist in New York, New York. Dr. Sawinski is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Chronic Kidney Disease, End-Stage Renal Disease (ESRD), High Potassium Level, Kidney Transplant, and Nephrectomy. Dr. Sawinski is currently accepting new patients.

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 Multiple Sulfatase Deficiency. His top areas of expertise are Hypotonia, Microcephaly, Achalasia Microcephaly Syndrome, and Cortical Dysplasia.

Lakshmi Mehta is a Medical Genetics provider in New York, New York. Dr. Mehta is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Microcephaly, Achalasia Microcephaly Syndrome, Hypotonia, and Acromicric Dysplasia. Dr. Mehta is currently accepting new patients.

Mary Lopiccolo is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Lopiccolo is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Glutaric Acidemia Type 2, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Carnitine Palmitoyltransferase 2 Deficiency.