Overview
Kenneth Rosenbaum is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Rosenbaum is rated as an Experienced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. His top areas of expertise are Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Triple X Syndrome, and Williams Syndrome. Dr. Rosenbaum is currently accepting new patients.
His clinical research consists of co-authoring 18 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- OTHER MEDICAID
- STATE MEDICAID
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
1 Clinical Trials
University Of Maryland Pediatric Associates, PA
Sofia Saenz-Ayala is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Saenz-Ayala is rated as an Advanced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. Her top areas of expertise are 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.
Children's Hospital
John Schreiber is a Pediatric Neurologist and a Neurologist in Washington, Washington, D.c.. Dr. Schreiber is rated as a Distinguished provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. His top areas of expertise are Epilepsy, Myoclonic Epilepsy, Seizures, and Epilepsy with Myoclonic-Atonic Seizures. Dr. Schreiber is currently accepting new patients.
Ryan Gill is a Pediatrics specialist and a Pediatric Neurologist in Baltimore, Maryland. Dr. Gill is rated as an Advanced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. Her top areas of expertise are Tuberous Sclerosis, Tuberous Sclerosis Complex, Sturge-Weber Syndrome, and West Syndrome.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- NeurofibromatosisDr. Rosenbaum isAdvanced. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)Dr. Rosenbaum isAdvanced. Learn about Neurofibromatosis Type 1 (NF1).
- Triple X SyndromeDr. Rosenbaum isAdvanced. Learn about Triple X Syndrome.
- Experienced
- 15q11.2 MicrodeletionDr. Rosenbaum isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Rosenbaum isExperienced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Rosenbaum isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Rosenbaum isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Rosenbaum isExperienced. Learn about 47 XYY Syndrome.
- Aarskog SyndromeDr. Rosenbaum isExperienced. Learn about Aarskog Syndrome.