Overview
Arupa Ganguly is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Ganguly is rated as an Experienced provider by MediFind in the treatment of Bannayan-Riley-Ruvalcaba Syndrome. Her top areas of expertise are Macroglossia, Beckwith-Wiedemann Syndrome, Mosaicism, Newborn Low Blood Sugar, and Tissue Biopsy.
Her clinical research consists of co-authoring 100 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Bannayan-Riley-Ruvalcaba Syndrome.
Insurance
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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.
Penn Translational Medicine And Human Genetics
Katherine Nathanson is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Nathanson is rated as a Distinguished provider by MediFind in the treatment of Bannayan-Riley-Ruvalcaba Syndrome. His top areas of expertise are Pheochromocytoma, Cowden Syndrome, Peutz-Jeghers Syndrome, and Hypothalamic Hamartomas. Dr. Nathanson is currently accepting new patients.
Jennifer Kalish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kalish is rated as an Elite provider by MediFind in the treatment of Bannayan-Riley-Ruvalcaba Syndrome. Her top areas of expertise are Beckwith-Wiedemann Syndrome, Macroglossia, Hemi 3 Syndrome, Hemihyperplasia, and Glossectomy.
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
- Beckwith-Wiedemann SyndromeDr. Ganguly isElite. Learn about Beckwith-Wiedemann Syndrome.
- MacroglossiaDr. Ganguly isElite. Learn about Macroglossia.
- Distinguished
- Chromosome 11 Uniparental DisomyDr. Ganguly isDistinguished. Learn about Chromosome 11 Uniparental Disomy.
- MosaicismDr. Ganguly isDistinguished. Learn about Mosaicism.
- Newborn Low Blood SugarDr. Ganguly isDistinguished. Learn about Newborn Low Blood Sugar.
- OmphaloceleDr. Ganguly isDistinguished. Learn about Omphalocele.
- Advanced
- FG SyndromeDr. Ganguly isAdvanced. Learn about FG Syndrome.
- Hardikar SyndromeDr. Ganguly isAdvanced. Learn about Hardikar Syndrome.
- Experienced
- Acromicric DysplasiaDr. Ganguly isExperienced. Learn about Acromicric Dysplasia.
- Bannayan-Riley-Ruvalcaba SyndromeDr. Ganguly isExperienced. Learn about Bannayan-Riley-Ruvalcaba Syndrome.
- Cowden SyndromeDr. Ganguly isExperienced. Learn about Cowden Syndrome.
- Hereditary Hemorrhagic TelangiectasiaDr. Ganguly isExperienced. Learn about Hereditary Hemorrhagic Telangiectasia.
- IntersexDr. Ganguly isExperienced. Learn about Intersex.
- Lhermitte-Duclos DiseaseDr. Ganguly isExperienced. Learn about Lhermitte-Duclos Disease.