Overview
Seth Berger is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Berger is rated as an Experienced 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.
His clinical research consists of co-authoring 67 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article 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
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
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.
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.
Kenneth Rosenbaum is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Rosenbaum is rated as an Advanced 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.
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
- Distinguished
- Alpha ThalassemiaDr. Berger isDistinguished. Learn about Alpha Thalassemia.
- Fetal EdemaDr. Berger isDistinguished. Learn about Fetal Edema.
- Hemolytic Disease of the NewbornDr. Berger isDistinguished. Learn about Hemolytic Disease of the Newborn.
- HoloprosencephalyDr. Berger isDistinguished. Learn about Holoprosencephaly.
- Hydrops FetalisDr. Berger isDistinguished. Learn about Hydrops Fetalis.
- Advanced
- ALG9-CDGDr. Berger isAdvanced. Learn about ALG9-CDG.
- Early Infantile Epileptic Encephalopathy
- Experienced
- Achalasia Microcephaly SyndromeDr. Berger isExperienced. Learn about Achalasia Microcephaly Syndrome.
- ALG1-CDGDr. Berger isExperienced. Learn about ALG1-CDG.
- Aplasia Cutis CongenitaDr. Berger isExperienced. Learn about Aplasia Cutis Congenita.
- Arthrogryposis Multiplex CongenitaDr. Berger isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Autism Spectrum DisorderDr. Berger isExperienced. Learn about Autism Spectrum Disorder.
- Brittle Cornea SyndromeDr. Berger isExperienced. Learn about Brittle Cornea Syndrome.