The 20 Best Smith-Magenis Syndrome Doctors in The United States

Sarah Elsea is a Medical Genetics provider practicing medicine in Houston, Texas. Dr. Elsea is rated as an Elite provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 14 other conditions, according to our data. Her clinical expertise encompasses Smith-Magenis Syndrome, Potocki-Lupski Syndrome, Hypotonia, and Zellweger Syndrome.

Lorraine Potocki is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Houston, Texas. Dr. Potocki is rated as an Elite provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Potocki-Lupski Syndrome, Smith-Magenis Syndrome, Hypotonia, and Trisomy 17 Mosaicism. Dr. Potocki is currently accepting new patients.

. Dr. Russi is rated as an Advanced provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 125 other conditions, according to our data. His clinical expertise encompasses Increased Head Circumference, Ehlers-Danlos Syndrome (EDS), Chromosome 8p Deletion, and Chromosome 6q Duplication. Dr. Russi is board certified in American Board Of Pediatrics and American Board Of Medical Genetics.

. Dr. Perszyk is rated as an Advanced provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Mucolipidosis 3. Dr. Perszyk is board certified in American Board Of Medical Genetics And Genomics.

Laurie Seaver is a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Seaver is rated as an Advanced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses 1p36 Deletion Syndrome, Hypotonia, Smith-Magenis Syndrome, and Potocki-Lupski Syndrome. Dr. Seaver is currently accepting new patients.

William Wierda is a Hematologist and an Oncologist practicing medicine in Houston, Texas. Dr. Wierda is rated as a Distinguished provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 28 other conditions, according to our data. His clinical expertise encompasses Chronic B-Cell Leukemia (CBCL), Chronic Lymphocytic Leukemia (CLL), Leukemia, Bone Marrow Aspiration, and Bone Marrow Transplant.

Linda Rossetti is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 10 years. Dr. Rossetti is rated as an Advanced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 87 other conditions, according to our data. Her clinical expertise encompasses Smith-Magenis Syndrome, Miller-Dieker Syndrome, Chromosome 6q Duplication, and Chromosome 8p Deletion. Dr. Rossetti is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Hyde Park, New York. Dr. Fernandes is rated as an Advanced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 153 other conditions, according to our data. Her clinical expertise encompasses Microcephaly, Chromosome 13q Deletion, Hennekam Syndrome, and Acrodermatitis Enteropathica.

Elizabeth Roeder is a Medical Genetics provider practicing medicine in San Antonio, Texas. Dr. Roeder is rated as an Advanced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Micrognathia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Smith-Magenis Syndrome, and Cornelia De Lange Syndrome. Dr. Roeder is board certified in American Board Of Medical Genetics And Genomics.

In my clinical practice, I see adult patients with diagnosed or suspected genetic disease. This includes both chromosomal abnormalities, as well as single gene disorders. I see patients with a variety of disorders, including Tuberous Sclerosis, Neurofibromatosis, connective tissue disease including Ehlers-Danlos syndrome and Marfan syndrome, and familial cancer syndromes. I have a particular clinical interest in patients with cardiopulmonary disease. As a physician-scientist, I have a research focus on postural orthostatic hypotension (POTS) and pulmonary artery hypertension (PAH). Dr. Posey is rated as an Advanced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Hypotonia, Achalasia Microcephaly Syndrome, Microcephaly, and Cortical Dysplasia. Dr. Posey is currently accepting new patients.

. Dr. Narumanchi is rated as an Experienced provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Narumanchi is board certified in American Board Of Medical Genetics And Genomics.

James Lupski is a Pediatrics provider practicing medicine in Houston, Texas. Dr. Lupski is rated as a Distinguished provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 37 other conditions, according to our data. His clinical expertise encompasses Potocki-Lupski Syndrome, Hypotonia, Achalasia Microcephaly Syndrome, and Microcephaly.

Bo Yuan is a Medical Genetics provider practicing medicine in Seattle, Washington. Dr. Yuan is rated as a Distinguished provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Potocki-Lupski Syndrome, Smith-Magenis Syndrome, Mosaicism, and Trisomy 17 Mosaicism.

Brett Graham is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Indianapolis, Indiana. Dr. Graham is rated as a Distinguished provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses MELAS Syndrome, Mitochondrial Complex 1 Deficiency, Smith-Magenis Syndrome, and Hypotonia. Dr. Graham is currently accepting new patients.

Matthew Davids is an Oncologist practicing medicine in Boston, Massachusetts. Dr. Davids is rated as a Distinguished provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 20 other conditions, according to our data. His clinical expertise encompasses Chronic Lymphocytic Leukemia (CLL), Chronic B-Cell Leukemia (CBCL), Small Lymphocytic Lymphoma (SLL), Bone Marrow Transplant, and Bone Marrow Aspiration.

William Gahl is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Bethesda, Maryland. Dr. Gahl is rated as a Distinguished provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Oculocutaneous Albinism Type 2, Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Type 1, Oculocutaneous Albinism, and Deep Brain Stimulation.

Diana Carrasco is a Medical Genetics provider practicing medicine in Fort Worth, Texas. Dr. Carrasco is rated as an Experienced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Trisomy 12 Mosaicism, Trisomy 14 Mosaicism, Trisomy 2 Mosaicism, and Trisomy 3 Mosaicism.

Dr. Julie Hoover-Fong is a Professor of Genetic Medicine and Pediatrics and Director of the Greenberg Center for Skeletal Dysplasias at Johns Hopkins University. Dr. Hoover-Fong holds a bachelor’s degree in Human Nutrition from The Ohio State University, where she also completed her medical degree. She received her Ph.D. in the Graduate Training Program in Clinical Investigation at the Johns Hopkins University School of Medicine and Bloomberg School of Public Health. Dr. Hoover-Fong completed a pediatric internship and residency at Washington University in St. Louis and a fellowship in medical genetics at Johns Hopkins University in Baltimore. She joined the Johns Hopkins University faculty in 2002 and progressed to Professor of Genetic Medicine and Pediatrics in 2019. She practices and oversees the clinical operations, research and educational ventures for the patients, families and healthcare providers served by the Greenberg Center. Her clinical team develops and improves diagnostic and treatment guidelines for comprehensive care of patients with all types of bone conditions including dwarfism, orofacial clefting, craniosynostosis and more. Dr. Hoover-Fong also mentors and teaches medical students, residents and genetic medicine trainees. As an active clinical researcher, Dr. Hoover-Fong is the Principal Investigator of multiple global clinical trials for achondroplasia, the first multi-center, investigator-initiated natural history study for achondroplasia, and multiple clinical studies for patients with orofacial clefting, hypophosphatasia and other conditions. She is also a co-investigator on the ELSI and Phenotype Review Committees for the Mendel Project, a whole exome sequencing venture to identify the genetic cause of Mendelian conditions. From an institutional service perspective, Dr. Hoover-Fong serves on the Johns Hopkins Associate Professor Promotions Committee and the Advisory Committee for the Graduate Training Program in Clinical Investigation. She serves on the Medical Advisory Board of the Little People of America, is a member of the Miller-Coulson Academy of Clinical Excellence at Johns Hopkins University and is a charter member of the International Skeletal Dysplasia Management Consortium, publishing best practice guidelines for patients with skeletal dysplasias. Dr. Hoover is rated as an Experienced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 26 other conditions, according to our data. Her clinical expertise encompasses Rhizomelic Syndrome, Achondroplasia, Spondyloepimetaphyseal Dysplasia Strudwick Type, Adenoidectomy, and Myringotomy. Dr. Hoover is board certified in American Board Of Medical Genetics And Genomics.

David Everman is a Medical Genetics provider practicing medicine in Greenville, South Carolina. Dr. Everman is rated as an Experienced provider by MediFind in the treatment of Smith-Magenis Syndrome. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Johanson-Blizzard Syndrome, Chromosome 2p Duplication, Ectodermal Dysplasias, and Clouston Syndrome. Dr. Everman is currently accepting new patients.

Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as an Experienced provider by MediFind in the treatment of Smith-Magenis Syndrome. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, and Progressive External Ophthalmoplegia. Dr. Vernon is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.