The 20 Best Multiple Sulfatase Deficiency Doctors Near Me

Lars Schlotawa practices in Goettingen, Germany. Mr. Schlotawa is rated as an Elite expert by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Multiple Sulfatase Deficiency, Metachromatic Leukodystrophy, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, CACH Syndrome, and Thrombectomy.

Rebecca Ahrens is a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ahrens is rated as an Elite provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Multiple Sulfatase Deficiency, Cardiomyopathic Lentiginosis, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, and Noonan Syndrome.

. Dr. Russi is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Increased Head Circumference, Ehlers-Danlos Syndrome (EDS), Chromosome 8p Deletion, and Chromosome 6q Duplication.

Sonia Christian is a Hematologist and an Oncologist in Chicago, Illinois. Dr. Christian is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Thrombocytopenia, Gallbladder Adenocarcinoma, Gallbladder Cancer, Pulmonary Embolism, and Bone Marrow Aspiration.

. Dr. Musgrave is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Paget Disease of the Breast, Thrombocytopenia, Neuroendocrine Tumor, and Angiosarcoma.

Brad Angle is a Medical Genetics provider in Park Ridge, Illinois. Dr. Angle is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are KBG Syndrome, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Cortical Dysplasia, and Micrognathia.

Adam Siegel is a Hematologist and an Oncologist in Summit, Wisconsin. Dr. Siegel is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Chronic T-Cell Leukemia (CTCL), Adult T-Cell Leukemia, Angiosarcoma, and Inflammatory Breast Cancer.

Angelika Erwin is a Pediatrics provider in Cleveland, Ohio. Dr. Erwin 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.

. Dr. Poobalasingham is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Acute Kidney Failure, Chronic Kidney Disease, Nephrosclerosis, Renovascular Hypertension, and Gastrostomy.

Kenneth Nahum is a Hematologist Oncology provider in Howell, New Jersey. Dr. Nahum is rated as a Distinguished provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Colorectal Cancer, Familial Colorectal Cancer, Lynch Syndrome, Bone Marrow Aspiration, and Fasciotomy.

Andres Giraldo is a primary care provider, practicing in Internal Medicine in Lincolnwood, Illinois. Dr. Giraldo is rated as an Experienced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Splenomegaly, Obesity, Hypertension, and Familial Hypertension.

Ahmad Tuffaha is a Nephrologist in Overland Park, Kansas. Dr. Tuffaha has been practicing medicine for over 21 years and is rated as a Distinguished provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Fabry Disease, End-Stage Renal Disease (ESRD), Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Kidney Transplant. Dr. Tuffaha is currently accepting new patients.

Eric Wallace is a Nephrologist in Birmingham, Alabama. Dr. Wallace is rated as a Distinguished provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Fabry Disease, Chronic Kidney Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Thrombectomy.

Raymond Wang is a Medical Genetics provider in Orange, California. Dr. Wang is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.

William Wilcox is a Medical Genetics provider in Atlanta, Georgia. Dr. Wilcox has been practicing medicine for over 38 years and is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Fabry Disease, Achondroplasia, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).

Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation.

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 Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Adrenoleukodystrophy (ALD), Leukodystrophy, Pelizaeus-Merzbacher Disease, and Alexander Disease.

Francis Senecal is an Oncologist in Tacoma, Washington. Dr. Senecal is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Paget Disease of the Breast, Breast Cancer, Angiosarcoma, Inflammatory Breast Cancer, and Bone Marrow Aspiration. Dr. Senecal is currently accepting new patients.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 8 years and is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.

Damara Ortiz, MD, specializes in medical genetics and pediatric genetics and genomics and is board-certified in pediatrics by the American Board of Pediatrics and clinical genetics by the American Board of Medical Genetics and Genomics. She is affiliated with UPMC Children's Hospital of Pittsburgh, UPMC Magee-Womens Hospital and UPMC Presbyterian. Dr. Ortiz completed her fellowship at Icahn School of Medicine at Mount Sinai, residency at NYU Langone Medical Center and medical degree from the University of Medicine and Dentistry of New Jersey Robert Wood Johnson Medical School. Dr. Ortiz is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Fabry Disease, Multiple Sulfatase Deficiency, Megalencephalic Leukoencephalopathy with Subcortical Cysts, and Gaucher Disease Type 1.