The 20 Best Prader-Willi Syndrome Doctors Near Me in Baltimore, MD

Dr. Eric Kossoff focuses on the diagnosis and treatment of childhood seizures and epilepsy, particularly treatments other than medications such as diet and neurostimulation. He is one of the world experts on dietary treatment for epilepsy (ketogenic diet) and lectures around the world about this therapy. His specific interests include the ketogenic diet, the modified Atkins diet for children and adults, infantile spasms, benign rolandic epilepsy, the interaction of migraine headaches with epilepsy, and Sturge-Weber syndrome. Dr. Eric Kossoff is also very involved in teaching and is the Director of the Pediatric Neurology Residency Program. He is a professor of neurology and pediatrics at the Johns Hopkins University School of Medicine. He is a co-author of Treatment of Pediatric Neurologic Disorders and the 7th edition of Ketogenic Diet Therapies. Dr. Kossoff sees patients in the Johns Hopkins Outpatient Center (5th floor) in Baltimore on Tuesday afternoons and Thursday mornings. He sees patients at Green Spring Station on Wednesday afternoons. He also participates in telemedicine. Dr. Kossoff received his medical degree from SUNY at Buffalo School of Medicine in New York. He went on to complete a residency in pediatrics at Eastern Virginia Medical School in Norfolk, Virginia. He completed a second residency in child neurology and a fellowship in pediatric epilepsy and clinical neurophysiology at The Johns Hopkins Hospital in Baltimore. Dr. Kossoff is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Epilepsy, Epilepsy in Children, Seizures, Endovascular Embolization, and Gastrostomy. Dr. Kossoff is board certified in American Board Of Psychiatry And Neurology.

Dr. Adam Hartman is an Adjunct Associate Professor of Neurology and Pediatrics at Johns Hopkins School of Medicine. He focuses on treating children with epilepsy, with an emphasis on those whose seizures have not been adequately controlled with medication. He evaluates and manages patients in his clinic who may be candidates for epilepsy surgery, including those with Rasmussen syndrome, brain malformations, and perinatal strokes. Patients who may not be surgery candidates due to inborn errors of metabolism (particularly mitochondrial disorders) also are a special interest for Dr. Hartman. Dr. Hartman is currently a Physician at NINDS/NIH, serving as a Program Director in the Division of Clinical Research. Previously, Dr. Hartman was the Associate Program Director for the Pediatric Neurology Residency at Johns Hopkins Hospital. He also was the Co-Director of the Neurology Intensive Care Nursery and an Attending Physician on the Pediatric Neurology Inpatient Service at Johns Hopkins Hospital. Dr. Hartman’s prior laboratory work was funded by National Institute of Neurological Disorders and Stroke (NIH), Technology Development Corporation (State of Maryland), a Johns Hopkins University School of Medicine Clinician Scientist Award, the Pakula Family, and the Becker Family. Dr. Hartman received his medical degree from Northwestern University Medical School. After completing his residency in Pediatrics in the National Capital Uniformed Services Pediatric Residency Program (National Naval Medical Center, Walter Reed Army Medical Center), he served as a general pediatrician in the US Navy for five years (the last as division head of general pediatrics at Naval Medical Center San Diego). He completed his residency in pediatric neurology and a fellowship in clinical neurophysiology/pediatric epilepsy, both at Johns Hopkins. Dr. Hartman is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Hemimegalencephaly, Seizures, Epilepsy, and Increased Head Circumference. Dr. Hartman is board certified in American Board Of Psychiatry And Neurology.

Dr. Ann O'Shea Scheimann is an associate professor of pediatrics at the Johns Hopkins University School of Medicine. Her areas of clinical expertise include pediatric gastroenterology, nutrition and pediatric liver disease including cholestatic liver disease and fatty liver disease. Dr. Scheimann received her B.S. from the University of Dayton. She earned her M.D. from the University of Cincinnati College of Medicine and her M.B.A. from Johns Hopkins. She completed her internship and residency in pediatric medicine and a fellowship in pediatric gastroenterology at the Baylor College of Medicine. In 2000, she joined the Johns Hopkins faculty in pediatrics, where her research focuses on non-alcoholic fatty liver disease, obesity and Prader-Willi syndrome. Prior to joining Johns Hopkins, Dr. Scheimann was an assistant professor of pediatrics at Baylor College of Medicine. In 2005, she developed Weigh Smart, a comprehensive pediatric weight management program funded by the Johns Hopkins Children’s Center, Mt. Washington Pediatric Hospital, and the University of Maryland. She currently serves as the chair of the Pediatric Nutrition Advisory Committee at Johns Hopkins Children's Center. Dr. Scheimann serves on the editorial boards of Pediatrics and Therapeutics, World Journal of Gastroenterology and World Journal of Hepatology. She has received numerous awards and including a grant from the Mt. Washington Pediatric Foundation to start the Weigh Smart program. She has received research support from Agencies including the National Institutes of Health, Foundation for Prader-willi Research and Prader-willi Syndrome Association. She is a member of several professional organizations, including the American Association for the Advancement of the Study of Liver Disease, Obesity Society and the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Dr. Scheimann is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. Her clinical expertise encompasses Delayed Growth, Obesity, Prader-Willi Syndrome, and Non-Alcoholic Fatty Liver Disease. Dr. Scheimann is board certified in American Board Of Pediatrics.

Dr. Garry R. Cutting is a Professor of Pediatrics and Medicine in the McKusick-Nathans Institute of Genetic Medicine of the Johns Hopkins University School of Medicine. He is the Aetna/U.S. Healthcare Professor of Medical Genetics at Johns Hopkins. Dr. Cutting received his undergraduate degree in biology and medical degree from the University of Connecticut. He completed residency training in pediatrics and a fellowship in medical genetics at the Johns Hopkins University School of Medicine. Dr. Cutting is the Medical Director of the DNA Diagnostic Laboratory of Johns Hopkins Genomics. He directed the Medical Genetics Residency Program at Hopkins from 1995 to 2004. Dr. Cutting is the recipient of the Paul di Sant’Agnese Distinguished Scientific Achievement Award from the Cystic Fibrosis Foundation and a MERIT award from the National Institutes of Health. He has published more than 160 peer-reviewed articles. Dr. Cutting was elected to the Society of Pediatric Research (1992), the American Society of Clinical Investigation (1995) and the Association of American Physicians (2017). Dr. Cutting’s primary interests lie in the interpretation of DNA variation and their effect upon human phenotypes. Dr. Cutting’s lab focuses on the effect of common and rare variants in the CFTR gene that cause the single gene disorder cystic fibrosis (CF). His lab operates the CFTR2 database, a resource composed of clinical and genetic data on almost 90,000 individuals with CF world-wide. His laboratory also studies the effect of clinically approved and novel modulators upon CFTR protein bearing disease-causing variants. Dr. Cutting’s laboratory is also leader in the identification and characterization of genetic modifiers of cystic fibrosis. His group is currently collaborating with teams at the University of North Carolina and the University of Washington, Seattle to identify common and rare modifier variants of disease severity by whole genome sequencing of 5200 individuals with CF. Dr. Cutting participates in the clinical translation of variant interpretation as the Medical Director of the DNA Diagnostic Laboratory at Johns Hopkins. Finally, as Editor of the journal Human Mutation Dr. Cutting oversees the review and publication of manuscripts reporting the mechanism, distribution and phenotype consequences of variation in our genomes. Dr. Cutting is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Exocrine Pancreatic Insufficiency, Russell-Silver Dwarfism, SHORT Syndrome, and Cornelia De Lange Syndrome. Dr. Cutting is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Thomas Traill is a Cardiologist practicing medicine in Baltimore,, Maryland. Dr. Traill is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Marfan Syndrome, Congenital Contractural Arachnodactyly, Arachnodactyly, and Bicuspid Aortic Valve.

Sally Radovick is a Pediatric Endocrinologist practicing medicine in Baltimore, Maryland. Dr. Radovick is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Panhypopituitarism, Pediatric Growth Hormone Deficiency, Growth Hormone Deficiency (GHD), and Obesity.

Dr. Stacy Fisher is a cardiologist in Baltimore, Maryland specializing in the care of adult congenital heart disease, pregnancy-related heart disease and congenital heart pulmonary hypertension. She is Associate Director of the Adult Congenital Heart Disease (ACHD) Center at the Johns Hopkins Heart and Vascular Institute and Director of the ACHD Training Program. She is also an Associate Professor of Medicine at the Johns Hopkins University School of Medicine. Her research focus is congenital heart disease in adults including pulmonary hypertension, inherited heart disease and 3D printing translational medicine. She is interested in imaging and using 3D modeling to advance cardiac care and education. Her education includes a Bachelor of Science degree in Microbiology from Miami University in Oxford, Ohio, and a Doctor of Medicine Degree from the University of Maryland School of Medicine in Baltimore, Maryland. She completed an internship and residency in Internal Medicine at Duke University in Durham, North Carolina. Her fellowship in cardiology was at the University of Rochester, Strong Memorial Hospital in Rochester, New York, including serving as the Chief Cardiology Fellow. She was then an Adult Congenital Heart Fellow at the University of Rochester, Strong Memorial Hospital. After completing her fellowship in 2001, she joined a Baltimore cardiology practice and was named Director of Women’s Cardiovascular Services and the Co-Director of the Cardiac Critical Care Unit at Sinai Hospital in Baltimore, positions which she held until 2011. She then joined University of Maryland School of Medicine as Director of Women’s and Complex Heart diseases where she started and directed the Adult Congenital Heart Program and practiced through 2022 when she joined Johns Hopkins. She was recently the President of the American Heart Association’s Greater Maryland Region. Videos Dr. Stacy Fisher. Dr. Fisher is rated as an Advanced provider by MediFind in the treatment of Prader-Willi Syndrome. She is also highly rated in 38 other conditions, according to our data. Her clinical expertise encompasses Familial Ventricular Tachycardia, Arrhythmias, Ventricular Tachycardia, Aortic Valve Replacement, and Transcatheter Aortic Valve Replacement (TAVR). Dr. Fisher is board certified in American Board Of Internal Medicine.

Walter Kaufmann is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Kaufmann is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Rett Syndrome, Fragile X Syndrome, Autism Spectrum Disorder, and Stereotypic Movement Disorder.

Hans Bjornsson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Bjornsson is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Kabuki Syndrome, Weaver Syndrome, Coffin-Lowry Syndrome, Stickler Syndrome, and Orchiectomy. Dr. Bjornsson is currently accepting new patients.

Debra Counts is a Pediatric Endocrinologist practicing medicine in Baltimore, Maryland. Dr. Counts is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. She is also highly rated in 19 other conditions, according to our data. Her clinical expertise encompasses Idiopathic Short Stature (ISS), Klinefelter Syndrome, Short Stature (Growth Disorders), and Pediatric Growth Hormone Deficiency.

Latricia Cook is a primary care provider, practicing in Internal Medicine in Owings Mills, Maryland. Dr. Cook is rated as an Advanced provider by MediFind in the treatment of Prader-Willi Syndrome. She is also highly rated in 31 other conditions, according to our data. Her clinical expertise encompasses Pena-Shokeir Syndrome Type 2, Prader-Willi Syndrome, Camptodactyly Syndrome Guadalajara Type 1, and Seckel Syndrome.