The 20 Best Wildervanck Syndrome 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 Wildervanck Syndrome. His top areas of expertise are Snyder-Robinson Syndrome, Abruzzo-Erickson Syndrome, Costello Syndrome, and WAGR 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 Wildervanck Syndrome. His top areas of expertise are Adrenoleukodystrophy (ALD), Leukodystrophy, Pelizaeus-Merzbacher Disease, and Alexander Disease.

Dr. Probasco is a professor at the Johns Hopkins University School of Medicine Department of Neurology. He is the Vice Chair for Quality, Safety, and Service for the department. He also serves as the Director of the Johns Hopkins Division of Advanced Clinical Neurology as well as the Medical Director of the Johns Hopkins Inpatient General Neurology Service. He co-directs the Johns Hopkins Encephalitis Center and the Johns Hopkins Center for Refractory Status Epilepticus and Neuroinflammation. He cares for general neurology inpatients and outpatients, specializing in autoimmune and paraneoplastic syndromes as well as neurological immune-related adverse events following immunotherapies for cancer. After completing his undergraduate studies in biochemistry at the University of New Mexico, Dr. Probasco attended the University of Oxford as a Rhodes Scholar and earned a second undergraduate degree in psychology, philosophy and physiology. He went on to earn his medical degree at the University of California, San Francisco. He completed an internship in internal medicine at Johns Hopkins Bayview Medical Center and a residency in neurology at Johns Hopkins, where he was the faculty liaison/executive chief resident. He went on to complete an instructorship in inpatient general neurology at Johns Hopkins. Dr. Probasco’s research interests include increasing care value through improving outcomes, incorporation of patient experience of disease and treatment, the efficiency of care delivery, and diagnostic test utilization in general and specifically in relation to autoimmune and paraneoplastic neurological syndromes, including encephalitis. Finally, he is interested in the management of neurological immune-related adverse events following immunotherapies for the treatment of cancer. Dr. Probasco has been recognized at the departmental, institutional, and national levels for teaching and clinical excellence, including the American Academy of Neurology’s A.B. Baker Teacher Recognition Award and the Frank L. Coulson, Jr. Award from the Johns Hopkins Medicine Miller-Coulson Academy of Clinical Excellence. He is a past graduate of the Johns Hopkins Armstrong Institute Resident Scholars (AIRS) program in Patient Safety and Quality. As a faculty member, he was inducted into the Miller-Coulson Academy of Clinical Excellence in 2019. He serves as Editor-in-Chief of NEJM Journal Watch Neurology. Videos The impact of COVID-19 on the Department of Neurology‚Äôs clinical care and medical education programs. Dr. Probasco is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. His top areas of expertise are Encephalitis, Anti-NMDA Receptor Encephalitis, Status Epilepticus, Creutzfeldt-Jakob Disease, and Gastrostomy.

Heather Brown is a Palliative Medicine provider in Baltimore, Maryland. Dr. Brown is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are CHARGE Syndrome, Early Infantile Epileptic Encephalopathy, Koolen De Vries Syndrome, and Microcephaly Deafness Syndrome.

Dr. Shruti Paranjape attended the University of Pennsylvania and received her M.D. from the University of Pittsburgh. She completed her pediatrics residency and pediatric pulmonology fellowship at Children’s Hospital of Pittsburgh. She has served as the Assistant Director of the CF Center at Children’s Hospital of Pittsburgh. Her awards include the James Sutherland Award for Outstanding Research by a Young Investigator. Dr. Paranjape is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Cystic Fibrosis, Secondary Immunodeficiency (SID), Newborn Jaundice, and Jaundice.

Dr. Elrick specializes in the care of children with neuromuscular disorders, and EMG studies in children and adults. He has special interests in genetic neuromuscular and neurodegenerative disorders and Acute Flaccid Myelitis. Dr. Elrick earned his M.D. and Ph.D. in Neuroscience at the University of Michigan Medical School, studying inherited neurodegenerative disorders of childhood. He completed residency training in Pediatrics and Child Neurology, followed by a fellowship in Neuromuscular Medicine and Johns Hopkins before joining the faculty in 2019. Dr. Elrick's laboratory research interest is in understanding mechanisms of neurodegenerative disease, especially those affecting motor neurons. He studies disorders caused by genetic mutations in the nuclear pore complex, the main pathway for transport of material in and out of the nucleus of the cell, including Triple A Syndrome. He also participates in clinical research on Acute Flaccid Myelitis (AFM), aimed at understanding susceptibility to AFM in children, and defining clinical and EMG characteristics of illness and recovery in AFM. Dr. Elrick is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. His top areas of expertise are Cramp-Fasciculation Syndrome, Acute Flaccid Myelitis (AFM), Dysferlinopathy, and Duchenne Muscular Dystrophy.

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 Wildervanck Syndrome. Her top areas of expertise are Congenital Contractural Arachnodactyly, Marfan Syndrome, Arachnodactyly, and Vici Syndrome.

After completing her bachelors of science degree in biochemistry from the City College of New York (CUNY), Dr. Smith-Hicks entered the Medical Scientist Training Program at Columbia University College of Physicians and Surgeons, where she obtained her M.D., Ph.D. in 2000. She trained in Pediatrics at the Albert Einstein College of Medicine and completed her Neurology and Pediatric Neurology training at the Johns Hopkins University School of Medicine in 2005. Dr. Smith-Hicks trained as a post-doctoral fellow in the Department of Neuroscience at Johns Hopkins University School of Medicine under the guidance of Dr. Paul Worley. She joined the faculty at Kennedy Krieger Institute in 2010 where she now sees patients with Autism Spectrum Disorder and Rett Syndrome, while conducting basic science research exploring disorders of learning and memory. Dr. Smith is rated as an Advanced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Rett Syndrome, Ruvalcaba Syndrome, Autism Spectrum Disorder, and Early Infantile Epileptic Encephalopathy.

Mihee Bay is a Pediatrics provider in Baltimore, Maryland. Dr. Bay is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Autism Spectrum Disorder, Delayed Growth, Wildervanck Syndrome, and Early Infantile Epileptic Encephalopathy.

I am a pediatric neurologist with expertise in epilepsy and electroencephalography (EEG). My clinical and research interests include genetics of epilepsy, medical management of patients with intractable epilepsy and presurgical evaluation of patients who are candidates for epilepsy surgery. Dr. Gupta is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. His top areas of expertise are Benign Rolandic Epilepsy, Lennox-Gastaut Syndrome (LGS), Seizures, and Memory Loss.

Sarah Korth, M.D. is an instructor at the Johns Hopkins Department of Physical Medicine and Rehabilitation. She serves as an attending physician at The Johns Hopkins Hospital and the Kennedy Krieger Institute. Dr. Korth’s interests include neuroplasticity of the developing brain, maximizing mobility, spasticity management, neurogenic bowel and bladder management, and a whole-person approach to management of children and adults with congenital conditions, including cerebral palsy and spina bifida. Dr. Korth’s rehabilitation-focused care aims to help people with congenital and acquired disabilities reach their maximum function. Dr. Korth also has an ongoing interest in methods of decreasing health disparities in developing countries. While in medical school, Dr. Korth initiated and developed a sustainable-changes health program called The Paraiso Project in rural Dominican Republic that she actively continues to direct. Dr. Korth is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Myelomeningocele, Hydrocele, Cerebral Palsy, and Neurogenic Bowel.

Pediatric and neonatal neurologist Joseph Scafidi is a clinician-scientist with expertise in pre-term neonatal brain injury, hypoxic ischemia and neurodevelopmental disorders. He directs the Michael V. Johnston Center for Developmental Neuroscience at Kennedy Krieger Institute. Dr. Scafidi earned a degree in osteopathic medicine from the Philadelphia College of Osteopathic Medicine. He completed residency training in pediatrics at Rutgers University Medical School as well as in child neurology at Children’s National Hospital, where he also undertook fellowship training in neonatal neurology. Additionally, Dr. Scafidi was a postdoctoral research fellow in developmental neurobiology at Children’s National Research Institute. His research interests focus on understanding metabolic adaptations after perinatal brain injury in the acute and long-term recovery phases, specifically how different cell populations in different brain regions use energy after injury and how these adaptations or maladaptations affect the recovery process. As a practicing pediatric and neonatal neurologist, Dr. Scafidi is ideally positioned to facilitate bench-to-bedside therapies through his laboratory and to improve knowledge of disease by developing and testing bedside-to-bench, research-driven hypotheses. Dr. Scafidi is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. His top areas of expertise are Cerebral Hypoxia, Seizures, Benign Rolandic Epilepsy, Premature Infant, and Endovascular Embolization.

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

Megan Bone is a Neurologist in Baltimore, Maryland. Dr. Bone is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Autism Spectrum Disorder, HNRNPH2-Related Disorder, 15q11.2 Microdeletion, and Jacobsen Syndrome.

Dr. Hilary E. Gwynn is an instructor on the medical staff at Kennedy Krieger Institute in the Division of Neurology and Developmental Medicine. She teaches medical trainees and provides patient care at the Center for Development and Learning and on the Pediatric Rehabilitation Unit. She is also the site coordinator for the Johns Hopkins pediatric resident developmental disabilities rotation at the Kennedy Krieger Institute. Dr. Gwynn earned her medical degree at the University of Maryland School of Medicine in Baltimore, Maryland in 2000 and completed her pediatrics residency there in 2003. She subsequently joined the Kennedy Krieger Institute in 2003 to attend the fellowship in neurodevelopmental disabilities through the Kennedy Krieger Institute and Johns Hopkins University School of Medicine. Since graduation from the fellowship program in 2007, she has been an active member of the medical staff at Kennedy Krieger Institute. She teaches medical trainees and provides patient care at the Center for Development and Learning and on the Pediatric Rehabilitation Unit. She is also a member of the clinical staff of the Department of Pediatrics at Johns Hopkins School of Medicine. Contact for Research Inquiries 801 N. Broadway Baltimore, MD 21205 Phone: (443) 923-3246 Research Summary Dr. Gwynn's clinical and research interests include diagnosis and treatment of the child with developmental disability. She is also investigating medical training methodology as it applies to resident and fellow training in the practice of developmental medicine and child neurology. Dr. Gwynn is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Cerebral Palsy, Focal Dystonia, Spastic Diplegia Infantile Type, and Moebius Syndrome.

Eric Mallack is a Pediatric Neurologist and a Neurologist in Baltimore, Maryland. Dr. Mallack is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. His top areas of expertise are Adrenoleukodystrophy (ALD), CACH Syndrome, Early Infantile Epileptic Encephalopathy, and Leukodystrophy.

Heather Riordan is a Pediatric Neurologist in Baltimore, Maryland. Dr. Riordan is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Cerebral Palsy, Focal Dystonia, Transient Tic Disorder, Spastic Diplegia Infantile Type, and Rhizotomy.

Alfredo Noguera is a Neurologist in Baltimore, Maryland. Dr. Noguera is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. His top areas of expertise are Rasmussen Encephalitis, Seizures, Focal or Multifocal Malformations in Neuronal Migration, and Periventricular Heterotopia.

Dr. Anna Maria Wilms Floet is an assistant professor of pediatrics at the Johns Hopkins University School of Medicine. She practices general pediatrics at the Kennedy Krieger Institute and is associated with the Wendy Klag Center for Autism & Developmental Disabilities. Dr. Floet earned her M.D. from Leiden University Medical Center in The Netherlands. Dr. Floet is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Autism Spectrum Disorder, Delayed Growth, Developmental Dysphasia Familial, and Koolen De Vries Syndrome.

Dr. Joanna Burton is a neurodevelopmental pediatrician at the Kennedy Krieger Institute and an assistant professor in the Department of Neurology at the Johns Hopkins School of Medicine. Dr. Burton graduated with honors with a bachelor’s degree in Linguistics from the University of Chicago in 1994. She then taught bilingual special education in Washington, DC for 5 years. She received an MD/PhD in 2008 from the University of Illinois, with the PhD in speech and hearing science, focusing on language acquisition. She then trained in general pediatrics at the University of Maryland Medical Center before receiving specialized training in neurodevelopmental disabilities at the Kennedy Krieger Institute. She currently sees patient with attentional and language based learning difficulties in the Center for Developmental and Learning, focusing on the development concerns of children with complex medical needs and those with a history of perinatal brain injury. She also sees patient in the Neurorehabilitation Concussion Clinic and provides inpatient consultations for high risk infants at Johns Hopkins Hospital. Contact for Research Inquiries 801 N. Broadway Baltimore, MD 21205 Research Summary Dr. Burton's dissertation focused on the effects of environment on assessment of word learning. She is a member of the Neurosciences Intensive Care Nursery (NICN) at the Charlotte Bloomberg Children’s Hospital at the Johns Hopkins Hospital and co-director of the Study on perinatal brain injury recovery and outcome (SPROUT) research collaborative at Kennedy Krieger. She currently investigates the neurodevelopmental outcomes of premature infants and term infants with a history of hypoxic-ischemic encephalopathy. She is working to identify which factors best predict short and long-term neurodevelopment and behavior associated with difficulties in daily living and academic success, specifically in the areas of attention and language. She also works with multi-disciplinary teams to examine potential interventions to mitigate early brain injury in these infants. Dr. Burton is rated as an Experienced provider by MediFind in the treatment of Wildervanck Syndrome. Her top areas of expertise are Intraventricular Hemorrhage of the Newborn, Alternating Hemiplegia of Childhood, Premature Infant, and Multiple Epiphyseal Dysplasia.