Overview
Zeina Maani is a primary care provider, practicing in Internal Medicine in Providence, Rhode Island. Her top areas of expertise are Collins Pope Syndrome, Brittle Cornea Syndrome, and Osteosclerosis Autosomal Dominant.
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Insurance
Accepted insurance can change. Please verify directly with the provider.
Locations
593 Eddy St, Providence, RI 02903
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Frequently Asked Questions about Dr. Zeina Maani
How do I make an appointment with Dr. Zeina Maani?
You can book an appointment with Dr. Zeina Maani by calling their office at 401-444-8450. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Zeina Maani a top-rated expert for Collins Pope Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Zeina Maani is classified as an Experienced expert for Collins Pope Syndrome, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Zeina Maani specialize in?
While Dr. Zeina Maani is a Internal Medicine, they have specific expertise in Collins Pope Syndrome, Brittle Cornea Syndrome, and Osteosclerosis Autosomal Dominant. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Internal Medicine.
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
- Brittle Cornea SyndromeDr. Maani isExperienced. Learn about Brittle Cornea Syndrome.
- Collins Pope SyndromeDr. Maani isExperienced. Learn about Collins Pope Syndrome.
- Osteosclerosis Autosomal DominantDr. Maani isExperienced. Learn about Osteosclerosis Autosomal Dominant.