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 Prader-Willi Syndrome. 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. In particular, he has participated in 1 clinical trial in the study of Prader-Willi Syndrome.
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
Garry Cutting is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Cutting is rated as an Advanced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Exocrine Pancreatic Insufficiency, Sjogren-Larsson Syndrome, Pena-Shokeir Syndrome Type 2, and Robinow Syndrome. Dr. Cutting is currently accepting new patients.
Seth Berger is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Berger is rated as a Distinguished provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Fetal Edema, Hydrops Fetalis, Hemolytic Disease of the Newborn, and Alpha Thalassemia.
Marshall Summar is a Medical Genetics specialist and a Pediatrics provider in Chevy Chase, Maryland. Dr. Summar is rated as a Distinguished provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Propionic Acidemia, and Ornithine Translocase Deficiency.
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.