Overview
Areeg El-Gharbawy is a Medical Genetics specialist and an Endocrinologist in Durham, North Carolina. Dr. El-Gharbawy and is rated as an Experienced provider by MediFind in the treatment of Gangliosidosis. Her top areas of expertise are Von Gierke Disease, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Mitochondrial Trifunctional Protein Deficiency, and Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Dr. El-Gharbawy is currently accepting new patients.
Her clinical research consists of co-authoring 25 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Gangliosidosis.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Cigna
- Humana
- Piedmont
Locations
40 Duke Medicine Cir, Durham, NC 27710
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.
2 Clinical Trials
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Von Gierke Disease
- Advanced
- Glycogen Storage Disease Type 3
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Micrognathia
- Mitochondrial Trifunctional Protein Deficiency
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Andersen Disease
- Brachydactyly Mononen Type
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Chondrodystrophy
- Cornelia De Lange Syndrome
- Deafness Craniofacial Syndrome