The 20 Best Temple Syndrome Doctors Near Me in Maryland, US

Dr. Albayda is an Associate Professor of Medicine in the Division of Rheumatology. She is the Director of the Rheumatology Fellowship Program, as well as Director of the Musculoskeletal Ultrasound and Injection Clinic. Nationally, she is involved in MSK Ultrasound education and has expertise in arthritis and inflammatory myopathies. Her research focuses on imaging biomarkers in rheumatic diseases, developing muscle ultrasound, clinical phenotypes in myositis, as well as longitudinal care and therapeutics in inclusion body myositis. Dr. Albayda is rated as an Advanced provider by MediFind in the treatment of Temple Syndrome. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Dermatomyositis, Inclusion Body Myositis, Myositis, and Polymyositis. Dr. Albayda is board certified in American Board Of Internal Medicine.

I am a pediatric neurologist with expertise in epilepsy and electroencephalography (EEG). My clinical and research interests include genetics of epilepsy, medical management of patients with intractable epilepsy and presurgical evaluation of patients who are candidates for epilepsy surgery. Dr. Gupta is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Benign Rolandic Epilepsy, Lennox-Gastaut Syndrome (LGS), Seizures, and Memory Loss. Dr. Gupta is board certified in American Board Of Psychiatry And Neurology.

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 Temple Syndrome. She is also highly rated in 26 other conditions, according to our data. Her clinical expertise encompasses Achondroplasia, Rhizomelic Syndrome, Spondyloepimetaphyseal Dysplasia Strudwick Type, Adenoidectomy, and Myringotomy. Dr. Hoover is board certified in American Board Of Medical Genetics And Genomics.

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 Temple 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.

Amena Fine is a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Fine is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Adrenoleukodystrophy (ALD), CACH Syndrome, HNRNPH2-Related Disorder, and Canavan Disease.

Neil Porter is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Porter is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. He is also highly rated in 29 other conditions, according to our data. His clinical expertise encompasses Myasthenia Gravis, Multiple Mononeuropathy, Mononeuritis Multiplex, Riboflavin Transporter Deficiency Neuronopathy, and Gastrostomy.

Dr. Gill cares for children with epilepsy and developmental, behavioral or psychiatric challenges. Her research and clinical interests include tuberous sclerosis complex, EEG biomarker development, and the intersection of epilepsy, genetics, and neurodevelopment. Dr. Gill is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Tuberous Sclerosis Complex, Tuberous Sclerosis, Sturge-Weber Syndrome, and West Syndrome.

Kenneth Rosenbaum, MD, started with Children’s National Hospital in 1972 after completing his medical genetics training at Johns Hopkins University in 1971. Dr. Rosenbaum has consistently been voted the top physician at Children’s National over the past 10 years. Dr. Rosenbaum has overseen dysmorphic research projects at the National Institutes of Health, in Egypt, and here at Children’s National. Dr. Rosenbaum is the co-director of the Down Syndrome Clinic and the NF clinic. Dr. Rosenbaum is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Triple X Syndrome, and Williams Syndrome. Dr. Rosenbaum is board certified in Clinical Cytogenetics: American Board Of Medical Genetics And Genomics, 1982, Clinical Genetics (MD): American Board Of Medical Genetics And Genomics, 1982, and Pediatrics: American Board Of Pediatrics, 1976.

Michel Fayad, MD, was born in Beirut, Lebanon and went to medical school at the American University of Beirut (AUB). After training in pediatrics at the AUB, then in Phoenix, AZ and in neurology at Emory in Atlanta, GA, he went back to Beirut, and was on the faculty at AUB for eight years. Dr. Fayad moved to Boston Children's Hospital in 2001 and has been on the faculty there since. He has seen general neurology patients, with a special interest in headaches, concussions, developmental and behavioral problems, especially autism and tic disorder. Dr. Fayad is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Infant Epilepsy with Migrant Focal Crisis, Epilepsy in Children, Epilepsy with Myoclonic-Atonic Seizures, and Myoclonic Epilepsy. Dr. Fayad is board certified in American Board Of Psychiatry And Neurology, 1998.

Tara Saggar is a primary care provider, practicing in Internal Medicine in Clinton, Maryland. Dr. Saggar is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. Her clinical expertise encompasses Temple Syndrome, Tetrasomy 9p, Chromosome 6 Uniparental Disomy, and Pallister-Killian Mosaic Syndrome.

Sofia Saenz-Ayala is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Saenz-Ayala is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Musculocontractural Ehlers-Danlos Syndrome (mcEDS), Ehlers-Danlos Syndrome (EDS), Carnitine Palmitoyltransferase 2 Deficiency, and Carnitine Palmitoyltransferase 1 Deficiency. Dr. Saenz-Ayala is currently accepting new patients.

After completing her bachelors of science degree in biochemistry from the City College of New York (CUNY), Dr. Smith-Hicks entered the Medical Scientist Training Program at Columbia University College of Physicians and Surgeons, where she obtained her M.D., Ph.D. in 2000. She trained in Pediatrics at the Albert Einstein College of Medicine and completed her Neurology and Pediatric Neurology training at the Johns Hopkins University School of Medicine in 2005. Dr. Smith-Hicks trained as a post-doctoral fellow in the Department of Neuroscience at Johns Hopkins University School of Medicine under the guidance of Dr. Paul Worley. She joined the faculty at Kennedy Krieger Institute in 2010 where she now sees patients with Autism Spectrum Disorder and Rett Syndrome, while conducting basic science research exploring disorders of learning and memory. Dr. Smith is rated as an Experienced provider by MediFind in the treatment of Temple Syndrome. She is also highly rated in 79 other conditions, according to our data. Her clinical expertise encompasses Rett Syndrome, Ruvalcaba Syndrome, Autism Spectrum Disorder, and Early Infantile Epileptic Encephalopathy. Dr. Smith is board certified in American Board Of Psychiatry And Neurology.