Dr. Anthony Perszyk
Overview
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Dr. Perszyk is rated as an Experienced provider by MediFind in the treatment of Chromosome 10q Deletion. His top areas of expertise are Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Mucolipidosis 3.
His clinical research consists of co-authoring 2 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
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- HMO
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- PPO
- HMO
- PPO
- EPO
- HMO
- INDEMNITY
- PPO
- EPO
- HMO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
160 E Erie Ave, Philadelphia, PA 19134
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.
Nemours DuPont Hospital For Children
Karen Gripp is a Medical Genetics provider in Wilmington, Delaware. Dr. Gripp is rated as an Elite provider by MediFind in the treatment of Chromosome 10q Deletion. Her top areas of expertise are Costello Syndrome, RASopathies, Noonan Syndrome, and Cardiofaciocutaneous 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 Chromosome 10q Deletion. Her top areas of expertise are Neurofibromatosis Type 1 (NF1), Gaucher Disease Type 1, Fabry Disease, and Neurofibromatosis.
St. Christopher's Pediatric Associates Genetics - E. Erie Avenue
. Dr. Narumanchi is rated as an Advanced provider by MediFind in the treatment of Chromosome 10q Deletion. His top areas of expertise are Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia.
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
- Chromosome 13q DeletionDr. Perszyk isAdvanced. Learn about Chromosome 13q Deletion.
- Dihydropteridine Reductase Deficiency
- Ehlers-Danlos Syndrome (EDS)Dr. Perszyk isAdvanced. Learn about Ehlers-Danlos Syndrome (EDS).
- Fabry DiseaseDr. Perszyk isAdvanced. Learn about Fabry Disease.
- Fetal Alcohol Syndrome (FAS)Dr. Perszyk isAdvanced. Learn about Fetal Alcohol Syndrome (FAS).
- Maternal HyperphenylalaninemiaDr. Perszyk isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Experienced
- 2q37 Deletion SyndromeDr. Perszyk isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Perszyk isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Perszyk isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Perszyk isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Perszyk isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Perszyk isExperienced. Learn about Acrorenal Mandibular Syndrome.