Overview
Barbara Burton is a Medical Genetics specialist and a Pediatrics provider in Chicago, Illinois. Dr. Burton is rated as an Experienced provider by MediFind in the treatment of Micrognathia. Her top areas of expertise are Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Phenylketonuria (PKU), Mucopolysaccharidoses (MPS), and Cholesteryl Ester Storage Disease.
Her clinical research consists of co-authoring 138 peer reviewed articles and participating in 9 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Micrognathia.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- MANAGED MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
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.
9 Clinical Trials
George Hoganson is a Medical Genetics specialist and a Pediatrics provider in Chicago, Illinois. Dr. Hoganson is rated as an Advanced provider by MediFind in the treatment of Micrognathia. His top areas of expertise are Isovaleric Acidemia, Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.
Gifty Bhat is a Medical Genetics specialist and a Pediatrics provider in Chicago, Illinois. Dr. Bhat is rated as a Distinguished provider by MediFind in the treatment of Micrognathia. Her top areas of expertise are Microcephaly, HNRNPH2-Related Disorder, Chromosome 6q Duplication, and Chromosome 8p Deletion. Dr. Bhat is currently accepting new patients.
Advocate Children's Medical Group Genetics
Brad Angle is a Medical Genetics provider in Park Ridge, Illinois. Dr. Angle is rated as an Advanced provider by MediFind in the treatment of Micrognathia. His top areas of expertise are KBG Syndrome, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Cortical Dysplasia, and Micrognathia.
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
- Elite
- Cholesteryl Ester Storage Disease
- Lysosomal Acid Lipase Deficiency
- Mucopolysaccharidoses (MPS)Dr. Burton isElite. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Phenylketonuria (PKU)Dr. Burton isElite. Learn about Phenylketonuria (PKU).
- Distinguished
- Brachydactyly Mononen TypeDr. Burton isDistinguished. Learn about Brachydactyly Mononen Type.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Advanced
- Krabbe DiseaseDr. Burton isAdvanced. Learn about Krabbe Disease.
- Maternal HyperphenylalaninemiaDr. Burton isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Mucolipidosis 3Dr. Burton isAdvanced. Learn about Mucolipidosis 3.
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Experienced
- Adrenoleukodystrophy (ALD)Dr. Burton isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Alpha MannosidosisDr. Burton isExperienced. Learn about Alpha Mannosidosis.
- Autosomal Recessive Congenital Methemoglobinemia
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2