Overview
Ibrahim Elsharkawi is a Pediatrics specialist and a Medical Genetics provider in New York, New York. Dr. Elsharkawi is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. His top areas of expertise are MELAS Syndrome, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Tyrosinemia Type 2.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- HMO
- POS
- PPO
- HMO
- POS
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- 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
1428 Madison Ave, New York, NY 10029
Icahn School Of Medicine At Mount Sinai
Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Breilyn is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 3. Her top areas of expertise are Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Tyrosinemia Type 1.
Icahn School Of Medicine At Mount Sinai
Mary Lopiccolo is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Lopiccolo is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. Her top areas of expertise are Glutaric Acidemia Type 2, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Carnitine Palmitoyltransferase 1 Deficiency.
Icahn School Of Medicine At Mount Sinai
Jaya Ganesh is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Ganesh is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 3. Her top areas of expertise are Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Fabry Disease.
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
- Andersen DiseaseDr. Elsharkawi isAdvanced. Learn about Andersen Disease.
- Argininosuccinic AciduriaDr. Elsharkawi isAdvanced. Learn about Argininosuccinic Aciduria.
- Autosomal Recessive Congenital Methemoglobinemia
- Beta-Ketothiolase DeficiencyDr. Elsharkawi isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Biotinidase DeficiencyDr. Elsharkawi isAdvanced. Learn about Biotinidase Deficiency.
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Elsharkawi isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Arginase DeficiencyDr. Elsharkawi isExperienced. Learn about Arginase Deficiency.
- Carbamoyl Phosphate Synthetase 1 DeficiencyDr. Elsharkawi isExperienced. Learn about Carbamoyl Phosphate Synthetase 1 Deficiency.
- Classic GalactosemiaDr. Elsharkawi isExperienced. Learn about Classic Galactosemia.
- Delayed GrowthDr. Elsharkawi isExperienced. Learn about Delayed Growth.
- Galactose Epimerase DeficiencyDr. Elsharkawi isExperienced. Learn about Galactose Epimerase Deficiency.