Overview
Arti Pandya is a Medical Genetics specialist and a Pediatrics provider in Richmond, Virginia. Dr. Pandya is rated as an Experienced provider by MediFind in the treatment of Chromosome 22 Duplication. Her top areas of expertise are Deafness Craniofacial Syndrome, Oculodentodigital Dysplasia Dominant, Oculodentodigital Dysplasia, and Primary Carnitine Deficiency. Dr. Pandya is currently accepting new patients.
Her clinical research consists of co-authoring 27 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
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.
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
- Advanced
- Deafness Craniofacial SyndromeDr. Pandya isAdvanced. Learn about Deafness Craniofacial Syndrome.
- Experienced
- Acromicric DysplasiaDr. Pandya isExperienced. Learn about Acromicric Dysplasia.
- Chromosome 13q DeletionDr. Pandya isExperienced. Learn about Chromosome 13q Deletion.
- Crouzon SyndromeDr. Pandya isExperienced. Learn about Crouzon Syndrome.
- Maple Syrup Urine DiseaseDr. Pandya isExperienced. Learn about Maple Syrup Urine Disease.
- MicrophthalmiaDr. Pandya isExperienced. Learn about Microphthalmia.
- Oculodentodigital DysplasiaDr. Pandya isExperienced. Learn about Oculodentodigital Dysplasia.