The 20 Best Cornelia De Lange Syndrome Doctors Near Me in Baltimore, MD

Antonie Kline is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Kline is rated as an Elite provider by MediFind in the treatment of Cornelia De Lange Syndrome. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Cornelia De Lange Syndrome, Micrognathia, Ehlers-Danlos Syndrome (EDS), and Crouzon Syndrome. Dr. Kline is currently accepting new patients.

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. She is also highly rated in 22 other conditions, according to our data. Her clinical expertise encompasses Hypotonia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Focal or Multifocal Malformations in Neuronal Migration, and Spinocerebellar Ataxia Type 3. Dr. Baranano is board certified in American Board Of Psychiatry And Neurology.

Thomas Traill is a Cardiologist practicing medicine in Baltimore,, Maryland. Dr. Traill is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange 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.

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. 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.

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. 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.

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. He is also highly rated in 54 other conditions, according to our data. His clinical expertise encompasses Sitosterolemia, Hypertension, Familial Hypertension, and Glucocorticoid-Remediable Aldosteronism.

Ambroise Wonkam is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Baltimore, Maryland. Dr. Wonkam is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Anemia, Fragile X Syndrome, Pyle Disease, and Micrognathia.

Tamar Harel is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Harel is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. She is also highly rated in 8 other conditions, according to our data. Her clinical expertise encompasses Hypotonia, Arthrogryposis Multiplex Congenita, Congenital Contractures, and Charcot-Marie-Tooth Disease.

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

Marshall Summar is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chevy Chase, Maryland. Dr. Summar is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Propionic Acidemia, and Ornithine Translocase Deficiency.

Maximilian Muenke is a Medical Genetics provider practicing medicine in Bethesda, Maryland. Dr. Muenke is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Holoprosencephaly, Turner Syndrome, Corpus Callosum Agenesis, and Chromosome 7q Duplication.