Overview
Deepika Burkardt is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Burkardt is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Micrognathia, Weaver Syndrome, Polymicrogyria, and Intersex.
Her clinical research consists of co-authoring 15 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE ASSISTANCE PROGRAM
- MEDICARE MAPD
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- 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.
Nicholas Ah Mew is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Ah Mew is rated as a Distinguished provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), Maple Syrup Urine Disease, Argininosuccinic Aciduria, and Propionic Acidemia.
The Johns Hopkins Hospital
Hind Alsharhan is a Medical Genetics provider in Baltimore, Maryland. Dr. Alsharhan is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are ALG3-CDG, Ornithine Transcarbamylase Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, and Phenylketonuria (PKU).
Peter Mcguire is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Mcguire is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Coenzyme Q Cytochrome C Reductase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) 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
- Experienced
- Increased Head CircumferenceDr. Burkardt isExperienced. Learn about Increased Head Circumference.
- IntersexDr. Burkardt isExperienced. Learn about Intersex.
- Leigh SyndromeDr. Burkardt isExperienced. Learn about Leigh Syndrome.
- MicrognathiaDr. Burkardt isExperienced. Learn about Micrognathia.
- PolydactylyDr. Burkardt isExperienced. Learn about Polydactyly.
- PolymicrogyriaDr. Burkardt isExperienced. Learn about Polymicrogyria.