Overview
Francis Reynoso is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Reynoso is rated as an Experienced provider by MediFind in the treatment of VACTERL Association. Her top areas of expertise are Biotinidase Deficiency, Maple Syrup Urine Disease, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Argininosuccinic Aciduria.
Her clinical research consists of co-authoring 6 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- INSURANCE PLAN
- OTHER COMMERCIAL
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE SNP
- OTHER MEDICARE PART D
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- POS
- EPO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
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.
Dena Matalon is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Matalon is rated as a Distinguished provider by MediFind in the treatment of VACTERL Association. Her top areas of expertise are Campomelia Cumming Type, Microcephaly Deafness Syndrome, Coffin-Lowry Syndrome, and Nevoid Basal Cell Carcinoma Syndrome.
Center For Medical Genomics Office HGCC MDC
Nina Powell is a Pediatrics specialist and a Medical Genetics provider in Newark, Delaware. Dr. Powell is rated as an Advanced provider by MediFind in the treatment of VACTERL Association. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Increased Head Circumference, and Perlman Syndrome.
Penn Translational Medicine And Human Genetics
Staci Kallish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kallish is rated as a Distinguished provider by MediFind in the treatment of VACTERL Association. Her top areas of expertise are Neurofibromatosis Type 1 (NF1), Gaucher Disease Type 1, Fabry Disease, and Neurofibromatosis. Dr. Kallish is currently accepting new 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
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Argininosuccinic AciduriaDr. Reynoso isAdvanced. Learn about Argininosuccinic Aciduria.
- Biotinidase DeficiencyDr. Reynoso isAdvanced. Learn about Biotinidase Deficiency.
- Maple Syrup Urine DiseaseDr. Reynoso isAdvanced. Learn about Maple Syrup Urine Disease.
- Experienced
- 2q37 Deletion SyndromeDr. Reynoso isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Reynoso isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Reynoso isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Reynoso isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acro-Pectoro-Renal Field DefectDr. Reynoso isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- Acrodermatitis EnteropathicaDr. Reynoso isExperienced. Learn about Acrodermatitis Enteropathica.