Overview
Staci Kallish is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Kallish and is rated as an Advanced provider by MediFind in the treatment of Vascular Ehlers-Danlos Syndrome (VEDS). Her top areas of expertise are Gaucher Disease Type 1, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, and Fabry Disease.
Her clinical research consists of co-authoring 18 peer reviewed articles. 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
- Humana
Locations
3400 Civic Ctr Blvd 2, Medical Genetics Icm Program, Philadelphia, PA 19104
Additional Areas of Focus
Dr. Kallish has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
Reed Pyeritz is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Pyeritz and is rated as a Distinguished provider by MediFind in the treatment of Vascular Ehlers-Danlos Syndrome (VEDS). His top areas of expertise are Hereditary Hemorrhagic Telangiectasia, Arachnodactyly, Achard Syndrome, and Vascular Ehlers-Danlos Syndrome (VEDS).
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.
- Advanced
- Alkaptonuria
- Brittle Cornea Syndrome
- Chromosome 13q Deletion
- Ehlers-Danlos Syndrome (EDS)
- Fabry Disease
- Gaucher Disease
- Experienced
- 2q37 Deletion Syndrome
- 3MC Syndrome
- 47 XYY Syndrome
- Aase Syndrome
- Abruzzo-Erickson Syndrome
- Acrodermatitis Enteropathica