The 20 Best Mucopolysaccharidoses (MPS) Doctors Near Me in Maryland, US

Dr. Gerald Raymond is a clinical geneticist and neurologist at Johns Hopkins where he is also a professor of genetic medicine and neurology. He obtained his MD at the University of Connecticut and was trained in Pediatrics at Johns Hopkins Hospital and Neurology at the Mass. General Hospital. He received additional training in developmental neuropathology at the Universite Catholique de Louvain in Belgium and clinical genetics at the Harvard Program. Dr. Raymond’s research has been at the overlap of genetics and neurology with specific focus on peroxisomal disorders including adrenoleukodystrophy. He has been actively involved in newborn screening for ALD and in developing clinical follow-up programs. He has extensive experience in clinical management of neurogenetic issues including peroxisomal and lysosomal disorders. He presently serves as the Director of the Lysosomal Storage Disease program in the department of Genetic Medicine. Dr. Raymond is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses Adrenoleukodystrophy (ALD), Metachromatic Leukodystrophy, Farber Lipogranulomatosis, and CACH Syndrome. Dr. Raymond is board certified in American Board Of Medical Genetics And Genomics and American Board Of Psychiatry And Neurology.

Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). She is also highly rated in 28 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation. Dr. Hamosh is board certified in American Board Of Medical Genetics And Genomics.

Hind Alsharhan is a Medical Genetics provider practicing medicine in Baltimore, Maryland. Dr. Alsharhan is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses ALG3-CDG, Ornithine Transcarbamylase Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, and Phenylketonuria (PKU). Dr. Alsharhan is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

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 Mucopolysaccharidoses (MPS). 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.

Sairah Khan is a Pediatric Cardiologist practicing medicine in Silver Spring,, Maryland. Dr. Khan is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). Her clinical expertise encompasses Myocarditis, Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), and Cardiomyopathy.

Elizabeth Elliott is a Pediatrics provider practicing medicine in Silver Spring, Maryland. Dr. Elliott is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). Her clinical expertise encompasses Mucopolysaccharidoses (MPS).

Bhupender Yadav is a Pediatric Radiologist practicing medicine in Silver Spring, Maryland. Dr. Yadav is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). His clinical expertise encompasses Hirschsprung Disease, Pneumomediastinum, Congenital Athymia, and Blue Rubber Bleb Nevus Syndrome.

Tamanna Roshan-Lal is a Pediatrics provider practicing medicine in Chevy Chase, Maryland. Dr. Roshan-Lal is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Gaucher Disease Type 2, Gaucher Disease Type 3, Gaucher Disease, and Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A).

Maria Arroyo is a Pediatric Pulmonologist practicing medicine in Silver Spring, Maryland. Dr. Arroyo is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). Her clinical expertise encompasses Spinal Muscular Atrophy Type 2, Duchenne Muscular Dystrophy, Congenital Central Hypoventilation Syndrome, and Omphalocele.

Oscar Rodriguez is a Sleep Medicine provider practicing medicine in Silver Spring, Maryland. Dr. Rodriguez is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). His clinical expertise encompasses Congenital Central Hypoventilation Syndrome, Asthma in Children, Asthma, and Sleepwalking (Somnambulism).

Sahar Romem is a Pediatrics provider practicing medicine in Silver Spring, Maryland. Dr. Romem is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). Her clinical expertise encompasses Mucopolysaccharidoses (MPS).

Geovanny Perez is a Pediatric Pulmonologist practicing medicine in Silver Spring, Maryland. Dr. Perez is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). His clinical expertise encompasses Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A), and Asthma in Children.

Tanya Cothran is a Pediatrics provider practicing medicine in Gaithersburg, Maryland. Dr. Cothran is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidoses (MPS). She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Obesity in Children, Asthma in Children, Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), and Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A).