The 20 Best Saethre-Chotzen Syndrome Doctors Near Me in Maryland, US

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 Saethre-Chotzen 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.

Plastic and reconstructive surgeon Barkat Ali cares for patients requiring complex reconstructive surgery after trauma and cancer, or those seeking cosmetic plastic surgery such as body contouring. Dr. Ali has a wealth of surgical experience treating patients and a strong commitment to patient-centered care. Dr. Ali earned his medical degree from Agha Khan University Medical College in Pakistan, and completed residency programs in general surgery and plastic surgery at the University of New Mexico School of Medicine. He also completed fellowships in hand surgery at the Christine M. Kleinert Institute for Hand and Micro Surgery at the University of Louisville School of Medicine, and a fellowship in reconstructive microsurgery at Memorial Sloan Kettering Cancer Center. Dr. Ali is rated as an Experienced provider by MediFind in the treatment of Saethre-Chotzen Syndrome. His clinical expertise encompasses Saethre-Chotzen Syndrome, Apert Syndrome, Acrocephalopolydactyly, Glossectomy, and Mastectomy. Dr. Ali is board certified in American Board Of Surgery.

Dr. Nara Lygia De Macena Sobreira is an assistant professor at the McKusick-Nathans Department of Genetic Medicine at Johns Hopkins University School of Medicine. Her area of expertise is rare Mendelian phenotypes, analysis of next-generation sequencing, and functional testing of candidate causative variants. She earned her M.D. at the University of Pernambuco in Brazil. She finished her Ph.D. in Human Genetics at Johns Hopkins followed by a one-year postdoc also at Johns Hopkins School of Medicine. During her Ph.D., she worked with Dr. David Valle using next-generation sequencing to elucidate the molecular basis of rare Mendelian phenotypes and in 2010 she discovered PTPN11 as the gene responsible for metachondromatosis by using whole-genome sequencing. She completed residencies in clinical genetics at both Universidade Federal de Sao Paulo and Johns Hopkins. Her main clinical and research focus is on identifying the genetic bases of rare phenotypes, mainly, phenotypes associated with cartilage tumors and vascular anomalies (including Ollier disease and Maffucci syndrome), and on understanding the physiopathology of these phenotypes to identify pharmacological strategies to treat them. She has worked extensively on developing strategies to better analyze the variants identified by next-generation sequencing and on novel strategies for data sharing. She participated on the development of PhenoDB, a phenotypic and genomic database, and created PhenoDB Variant Analysis Tool used worldwide. She is also one of the creators of GeneMatcher, VariantMatcher, and one of the co-founders of the Matchmaker Exchange, all intended to share next-generation sequencing data. She has also worked extensively on functional studies that evaluate the possible pathogenic effects of the candidate causative variants. Recent News Articles and Media Coverage Living the Hopkins Mission Honorees, Johns Hopkins Medicine Successes in Characterizing Genes through GeneMatcher with Nara L. M. Sobreira, MD, PhD, Ambry Genetics (April 30, 2018) Enfermedades raras: el desafio es encontrar otros pacientes que tienen el mismo mal, Lun (26 de septiembre de 2019) 2021 Science Writers' Boot Camp, Johns Hopkins Medicine (June 7, 2021) Making the Perfect Match, Johns Hopkins Medicine (February 1, 2020). Dr. De Macena Sobreira is rated as an Experienced provider by MediFind in the treatment of Saethre-Chotzen Syndrome. She is also highly rated in 24 other conditions, according to our data. Her clinical expertise encompasses Spondyloepimetaphyseal Dysplasia Strudwick Type, Greenberg Dysplasia, Blepharophimosis, and Early Infantile Epileptic Encephalopathy. Dr. De Macena Sobreira is board certified in American Board Of Medical Genetics And Genomics.

David Weisman is a primary care provider, practicing in Internal Medicine in Baltimore, Maryland. Dr. Weisman is rated as an Experienced provider by MediFind in the treatment of Saethre-Chotzen Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses End-Stage Renal Disease (ESRD), Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), Glucocorticoid-Remediable Aldosteronism, and Tissue Biopsy.

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 Saethre-Chotzen 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.

Robert Lesko is a Plastic Surgeon practicing medicine in Baltimore, Maryland. Dr. Lesko is rated as an Experienced provider by MediFind in the treatment of Saethre-Chotzen Syndrome. His clinical expertise encompasses Craniosynostosis, Saethre-Chotzen Syndrome, Acrocephalopolydactyly, Osteotomy, and Abdominal Wall Surgery.