The 20 Best Chromosome 2 Uniparental Disomy Doctors Near Me in Maryland, US

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 Chromosome 2 Uniparental Disomy. He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Seizures, Benign Rolandic Epilepsy, Rett Syndrome, Lennox-Gastaut Syndrome (LGS), and Thrombectomy. Dr. Gupta is board certified in American Board Of Psychiatry And Neurology.

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 Chromosome 2 Uniparental Disomy. 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.

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 Chromosome 2 Uniparental Disomy. She is also highly rated in 80 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.

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 Chromosome 2 Uniparental Disomy. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Tuberous Sclerosis, Tuberous Sclerosis Complex, Sturge-Weber Syndrome, and West Syndrome.

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 Chromosome 2 Uniparental Disomy. 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 Farber Lipogranulomatosis.

Neil Porter is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Porter is rated as an Experienced provider by MediFind in the treatment of Chromosome 2 Uniparental Disomy. He is also highly rated in 29 other conditions, according to our data. His clinical expertise encompasses Myasthenia Gravis, Mononeuritis Multiplex, Multiple Mononeuropathy, Riboflavin Transporter Deficiency Neuronopathy, and Gastrostomy.

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 Chromosome 2 Uniparental Disomy. Her clinical expertise encompasses Chromosome 6 Uniparental Disomy, Chromosome 11 Uniparental Disomy, Chromosome 2 Uniparental Disomy, and Pallister-Killian Mosaic Syndrome.

Michael Fayad is a Pediatric Neurologist practicing medicine in Silver Spring, Maryland. Dr. Fayad is rated as an Experienced provider by MediFind in the treatment of Chromosome 2 Uniparental Disomy. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Epilepsy in Children, Infant Epilepsy with Migrant Focal Crisis, Epilepsy with Myoclonic-Atonic Seizures, and West 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 Chromosome 2 Uniparental Disomy. 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 1 Deficiency, and Carnitine Palmitoyltransferase 2 Deficiency. Dr. Saenz-Ayala is currently accepting new patients.