The 20 Best Polysyndactyly Cardiac Malformation Doctors near Baltimore, MD

Dr. Harry “Hal” Dietz is a professor of pediatrics, an associate professor of medicine and an assistant professor of neurological surgery at the Johns Hopkins University School of Medicine. He is the Victor A. McKusick Professor of Genetics and also serves as the director of the William S. Smilow Center for Marfan Syndrome Research. Recognized as the world’s leading authority on Marfan syndrome, Dr. Dietz conducted genomic mapping and research on therapeutic agents for deficiencies in the genetic protein fibrillin, which is linked to Marfan syndrome. His research contributions have made diagnosis of the condition patient-specific and accurate. He has received more than 50 national and international awards and honors, including the Antoine Marfan Award from the National Marfan Foundation and the Art of Listening Award from the American Heart Association. Dr. Dietz is an ad hoc reviewer for 19 different organizations, including the American Journal of Cardiology, the Archives of Pediatric and Adolescent Medicine, and the Journal of Clinical Investigation. Over more than two decades, Dr. Dietz has mentored 75 predoctoral and postdoctoral researchers. He has authored 282 original publications in peer-reviewed journals, 25 textbook chapters, and 239 abstracts, and has also delivered more than 440 lectures on Marfan syndrome and related genetic disorders. Dr. Dietz completed his B.S. at Duke University and received his M.D. from the SUNY Upstate School of Medicine. He completed a pediatric residency and a cardiology fellowship at Johns Hopkins University before joining the faculty in 1992. Dr. Dietz is rated as an Advanced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. His top areas of expertise are Snyder-Robinson Syndrome, Abruzzo-Erickson Syndrome, Costello Syndrome, and WAGR Syndrome.

Dr. Grant Anhalt is a professor of dermatology at the Johns Hopkins University School of Medicine. His areas of clinical expertise include autoimmune skin diseases and dermatoimmunology. Dr. Anhalt serves as the director of the Dermatoimmunology Laboratory at the Johns Hopkins School of Medicine. He received his undergraduate degree and his M.D. from the University of Manitoba. He completed a residency in internal medicine at the Health Sciences Center in Winnipeg, Canada and a residency in dermatology at the University of Michigan. He performed a fellowship in immunodermatology at the University of Michigan Medical Center. Dr. Anhalt joined the Johns Hopkins faculty in 1982. He was interim chair of the Department of Dermatology from 1996 to 2001. His research interests include autoimmunity, bullous skin diseases and pemphigus and pemphigoid. Dr. Anhalt serves on the medical advisory board for the International Pemphigus & Pemphigoid Foundation. He has been recognized as a top doctor in the Washington Post Magazine, Baltimore Magazine and Castle Connolly Guide. He is a member of several professional organizations, including the American Academy of Dermatology, American Dermatologic Association and American Society for Clinical Investigation. CV http://www.hopkinsmedicine.org/dermatology/our_experts/CV/Anhalt_CV_2014.docx. Dr. Anhalt is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. His top areas of expertise are Pemphigus Vulgaris, Pemphigus, Pemphigus Foliaceus, and Bullous Pemphigoid.

Eugene Park is a Dermatologist in Baltimore, Maryland. Dr. Park is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. Her top areas of expertise are Nijmegen Breakage Syndrome, Currarino Triad, Birt-Hogg-Dube Syndrome, and Branchiootorenal 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 Polysyndactyly Cardiac Malformation. His top areas of expertise are Adrenoleukodystrophy (ALD), Leukodystrophy, Pelizaeus-Merzbacher Disease, and Alexander Disease.

Dr. Jennifer Pardo Habashi is an assistant professor of pediatrics at the Johns Hopkins University School of Medicine. Her research focuses on cardiology. Dr. Habashi provides genetic cardiology services at the Center for Inherited Heart Disease at the Johns Hopkins Heart and Vascular Institute. She is currently evaluating the effectiveness of medications for the treatment of Marfan syndrome. Dr. Habashi received her undergraduate degree from Brown University. She earned her M.D. from the University of Maryland Medical School. She completed residencies at Montefiore Medical Center and Johns Hopkins. She performed a fellowship in pediatric cardiology at Johns Hopkins. Her work has been recognized with several awards, including a grant from the National Marfan Foundation for her research to help reduce the risks associated with pregnancy for women with Marfan syndrome. Dr. Pardo is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. Her top areas of expertise are Congenital Contractural Arachnodactyly, Marfan Syndrome, Arachnodactyly, and Vici Syndrome.

Carol Greene is a Pediatrics provider in Baltimore, Maryland. Dr. Greene is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. Her top areas of expertise are Musculocontractural Ehlers-Danlos Syndrome (mcEDS), MELAS Syndrome, Ehlers-Danlos Syndrome (EDS), and Coenzyme Q Cytochrome C Reductase Deficiency.

Julia Cadrin is a Cardiologist in Baltimore,, Maryland. Dr. Cadrin is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. Her top areas of expertise are Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, Cardiac Arrest, Familial Hypertrophic Cardiomyopathy, and Cardiac Ablation.

Daniel Judge is a Cardiologist in Baltimore, Maryland. Dr. Judge is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. His top areas of expertise are Cardiomyopathy, Transthyretin Amyloid Cardiomyopathy, Cardiac Amyloidosis, Heart Transplant, and Cardiac Ablation.

David Weisman is a primary care provider, practicing in Internal Medicine in Baltimore, Maryland. Dr. Weisman is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. His top areas of expertise are End-Stage Renal Disease (ESRD), Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), Glucocorticoid-Remediable Aldosteronism, and Tissue Biopsy.

Melvin Blanchard is a primary care provider, practicing in Internal Medicine in Towson, Maryland. Dr. Blanchard is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. His top areas of expertise are Chronic Pain, Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), and Hypertension.

Joyce Evans is a primary care provider, practicing in Family Medicine in Columbia, Maryland. Dr. Evans is rated as an Experienced provider by MediFind in the treatment of Polysyndactyly Cardiac Malformation. Her top areas of expertise are Autonomic Neuropathy, Beare-Stevenson Cutis Gyrata Syndrome, Cohen Syndrome, and Alstrom Syndrome.