Overview
Arupa Ganguly is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Ganguly is rated as a Distinguished provider by MediFind in the treatment of Newborn Low Blood Sugar. 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 4 articles in the study of Newborn Low Blood Sugar.
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.
Jennifer Kalish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kalish is rated as an Elite provider by MediFind in the treatment of Newborn Low Blood Sugar. Her top areas of expertise are Beckwith-Wiedemann Syndrome, Macroglossia, Hemi 3 Syndrome, Hemihyperplasia, and Glossectomy.
Georgianne Arnold is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Arnold is rated as an Advanced provider by MediFind in the treatment of Newborn Low Blood Sugar. Her top areas of expertise are Phenylketonuria (PKU), Mitochondrial Trifunctional Protein Deficiency, Krabbe Disease, and Inborn Amino Acid Metabolism Disorder.
Childrens Health Care Associates Inc
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ficicioglu is rated as a Distinguished provider by MediFind in the treatment of Newborn Low Blood Sugar. His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
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.