Overview
Marwan Shinawi is a Medical Genetics specialist and a Pediatrics provider in Saint Louis, Missouri. Dr. Shinawi and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Hypotonia, Polysyndactyly Cardiac Malformation, Osteopathia Striata Cranial Sclerosis, and Increased Head Circumference. Dr. Shinawi is currently accepting new patients.
His clinical research consists of co-authoring 152 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Cigna
- Cox Health
- Humana
Locations
1 Childrens Pl, Saint Louis, MO 63110
13001 N Outer 40 Rd, 2e St Louis Childrens Specialty Care Cent, Town And Country, MO 63017
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.
1 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.
- Elite
- Hypotonia
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Achalasia Microcephaly Syndrome
- Acromicric Dysplasia
- Angelman Syndrome
- Argininosuccinic Aciduria
- Arthrogryposis Multiplex Congenita
- Experienced
- Andersen Disease
- Bannayan-Riley-Ruvalcaba Syndrome
- Brachydactyly Mononen Type
- Cat Eye Syndrome
- Chondrodystrophy
- Cornelia De Lange Syndrome