Overview
Elizabeth Streeten is an Endocrinologist and a Medical Genetics provider in Baltimore, Maryland. Dr. Streeten is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. Her top areas of expertise are Osteoporosis-Pseudoglioma Syndrome, Osteoporosis, Gaucher Disease, and Gaucher Disease Type 2.
Her clinical research consists of co-authoring 66 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
Additional Areas of Focus
Dr. Streeten has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
Johns Hopkins University
Hilary Vernon is a Pediatrics specialist and a Medical Genetics provider in Baltimore, Maryland. Dr. Vernon is rated as a Distinguished provider by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Progressive External Ophthalmoplegia, and Inborn Amino Acid Metabolism Disorder.
University Of Maryland Pediatric Associates, PA
Carol Greene is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Greene is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. Her top areas of expertise are Musculocontractural Ehlers-Danlos Syndrome (mcEDS), Phenylketonuria (PKU), Increased Head Circumference, and MELAS Syndrome.
Kimberly Chapman is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Chapman is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. Her top areas of expertise are Ehlers-Danlos Syndrome (EDS), Brittle Cornea Syndrome, Methylmalonic Acidemia, and Coenzyme Q Cytochrome C Reductase 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
- Elite
- Osteoporosis-Pseudoglioma Syndrome
- Advanced
- Brittle Cornea SyndromeDr. Streeten isAdvanced. Learn about Brittle Cornea Syndrome.
- Gaucher DiseaseDr. Streeten isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Streeten isAdvanced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Streeten isAdvanced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Streeten isAdvanced. Learn about Gaucher Disease Type 3.
- HypercalcemiaDr. Streeten isAdvanced. Learn about Hypercalcemia.
- Experienced
- Addison's DiseaseDr. Streeten isExperienced. Learn about Addison's Disease.
- Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED)
- Autoimmune Polyglandular Syndrome Type 2Dr. Streeten isExperienced. Learn about Autoimmune Polyglandular Syndrome Type 2.
- CalcinosisDr. Streeten isExperienced. Learn about Calcinosis.
- Coenzyme Q Cytochrome C Reductase Deficiency
- Defective Apolipoprotein B-100Dr. Streeten isExperienced. Learn about Defective Apolipoprotein B-100.