The 20 Best Cornelia De Lange Syndrome Doctors in Maryland, US

Antonie Kline is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Kline is rated as an Elite provider by MediFind in the treatment of Cornelia De Lange Syndrome. Her top areas of expertise are Cornelia De Lange Syndrome, Micrognathia, Ehlers-Danlos Syndrome (EDS), and Crouzon Syndrome. Dr. Kline is currently accepting new patients.

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 Cornelia De Lange Syndrome. Her top areas of expertise are Familial Ventricular Tachycardia, Arrhythmias, Ventricular Tachycardia, Aortic Valve Replacement, and Transcatheter Aortic Valve Replacement (TAVR).

Dr. Barañano earned her M.D. and Ph.D. degrees from the Johns Hopkins University School of Medicine, where she also completed residencies in pediatrics and neurology, along with a fellowship in neurogenetics at the Kennedy Krieger Institute. Dr. Barañano is an Associate Professor of Clinical Neurology. She specializes in the diagnosis and management of rare neurogenetic disorders. She has a particular interest in the genetic control and function of the cerebellum and expertise in childhood-onset and inherited ataxias. She is a member of the multidisciplinary Fetal Management group and is available for prenatal consultations. Dr. Barañano's research includes collaborative efforts with the Johns Hopkins Department of Genetic Medicine and the Division of Neurogenetics at the Kennedy Krieger Institute. Dr. Baranano is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. Her top areas of expertise are Hypotonia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Focal or Multifocal Malformations in Neuronal Migration, and Hereditary Ataxia.

Ambroise Wonkam is a Pediatrics specialist and a Medical Genetics provider in Baltimore, Maryland. Dr. Wonkam is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. His top areas of expertise are Anemia, Fragile X Syndrome, Pyle Disease, and Micrognathia.

Thomas Traill is a Cardiologist in Baltimore,, Maryland. Dr. Traill is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. His top areas of expertise are Marfan Syndrome, Congenital Contractural Arachnodactyly, Arachnodactyly, and Bicuspid Aortic Valve.

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 Cornelia De Lange Syndrome. His top areas of expertise are Exocrine Pancreatic Insufficiency, Sjogren-Larsson Syndrome, Prader-Willi Syndrome, and Pena-Shokeir Syndrome Type 2.

James Benke is a Cardiologist in Bel Air,, Maryland. Dr. Benke is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. His top areas of expertise are Cornelia De Lange Syndrome and Adenoidectomy.

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 Cornelia De Lange Syndrome. Her top areas of expertise are Robinow Syndrome, Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), and SHORT Syndrome.

Patrick Shanahan is a primary care provider, practicing in Family Medicine in Chestertown, Maryland. Dr. Shanahan is rated as an Advanced provider by MediFind in the treatment of Cornelia De Lange Syndrome. His top areas of expertise are Sitosterolemia, Familial Hypertension, Glucocorticoid-Remediable Aldosteronism, and Hypertension.

Doreen Blake is a primary care provider, practicing in Internal Medicine in Upper Marlboro, Maryland. Dr. Blake is rated as an Advanced provider by MediFind in the treatment of Cornelia De Lange Syndrome. Her top areas of expertise are Sitosterolemia, Familial Hypertension, Hypertension, and Glucocorticoid-Remediable Aldosteronism.

Natalie Blagowidow is a Medical Genetics specialist and an Obstetrics and Gynecologist in Baltimore, Maryland. Dr. Blagowidow is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. Her top areas of expertise are Immune Defect due to Absence of Thymus, Ehlers-Danlos Syndrome (EDS), DiGeorge Syndrome, and Cornelia De Lange Syndrome. Dr. Blagowidow is currently accepting new patients.

Tamar Harel is a Neurologist in Baltimore, Maryland. Dr. Harel is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. Her top areas of expertise are Hypotonia, Arthrogryposis Multiplex Congenita, Congenital Contractures, and Charcot-Marie-Tooth Disease.

Marshall Summar is a Medical Genetics specialist and a Pediatrics provider in Chevy Chase, Maryland. Dr. Summar is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. His top areas of expertise are Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Propionic Acidemia, and Ornithine Translocase Deficiency.

Maximilian Muenke is a Medical Genetics provider in Bethesda, Maryland. Dr. Muenke is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. His top areas of expertise are Holoprosencephaly, Turner Syndrome, Corpus Callosum Agenesis, and Chromosome 7q Duplication.