Overview
Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York.
Dr. Breilyn is highly rated in 42 conditions, according to our data. Her clinical expertise encompasses Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Phenylketonuria (PKU).
She is actively involved in clinical research, co-authoring 15 peer reviewed articles.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
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
- EPO
- HMO
- PPO
- EPO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- INSURANCE PLAN
- 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
1428 Madison Ave, New York, NY 10029
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.
Icahn School Of Medicine At Mount Sinai
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Robert Desnick is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Desnick is highly rated in 8 conditions, according to our data. His clinical expertise encompasses Hereditary Coproporphyria, Fabry Disease, Aplasia Cutis Congenita, and Ectodermal Dysplasias.
Elaine Pereira is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Pereira is highly rated in 7 conditions, according to our data. Her clinical expertise encompasses Chromosome 6q Deletion, Trisomy 13, Chromosome 13q Duplication, and Micrognathia.
Frequently Asked Questions about Dr. Margo S. Breilyn
How do I make an appointment with Dr. Margo S. Breilyn?
You can book an appointment with Dr. Margo S. Breilyn by calling their office at 212-241-6947. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Margo S. Breilyn a top-rated expert for Urea Cycle Disorders (UCD)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Margo S. Breilyn is classified as an Distinguished expert for Urea Cycle Disorders (UCD), meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Margo S. Breilyn specialize in?
While Dr. Margo S. Breilyn is a Medical Genetics, they have specific expertise in Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, and Short-Chain Acyl-CoA Dehydrogenase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Margo S. Breilyn participate in research or clinical trials?
Yes. Dr. Margo S. Breilyn has published 15 articles and abstracts on conditions like Urea Cycle Disorders (UCD). You can view a list of Dr. Margo S. Breilyn's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Margo S. Breilyn accept my insurance?
Dr. Margo S. Breilyn accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 212-241-6947 to verify that your specific plan is currently accepted before your visit.
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
- Distinguished
- Ornithine Transcarbamylase DeficiencyDr. Breilyn isDistinguished. Learn about Ornithine Transcarbamylase Deficiency.
- Phenylketonuria (PKU)Dr. Breilyn isDistinguished. Learn about Phenylketonuria (PKU).
- Short-Chain Acyl-CoA Dehydrogenase DeficiencyDr. Breilyn isDistinguished. Learn about Short-Chain Acyl-CoA Dehydrogenase Deficiency.
- Urea Cycle Disorders (UCD)Dr. Breilyn isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Von Gierke DiseaseDr. Breilyn isDistinguished. Learn about Von Gierke Disease.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Activated PI3K Delta Syndrome (APDS)
- Andersen DiseaseDr. Breilyn isAdvanced. Learn about Andersen Disease.
- Arginase DeficiencyDr. Breilyn isAdvanced. Learn about Arginase Deficiency.
- Argininosuccinic AciduriaDr. Breilyn isAdvanced. Learn about Argininosuccinic Aciduria.
- Beta-Ketothiolase DeficiencyDr. Breilyn isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Biotinidase DeficiencyDr. Breilyn isAdvanced. Learn about Biotinidase Deficiency.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- CitrullinemiaDr. Breilyn isAdvanced. Learn about Citrullinemia.
- Classic GalactosemiaDr. Breilyn isAdvanced. Learn about Classic Galactosemia.
- Dihydropteridine Reductase Deficiency
- Glutaric Acidemia Type 1Dr. Breilyn isAdvanced. Learn about Glutaric Acidemia Type 1.
- Glutaric Acidemia Type 2Dr. Breilyn isAdvanced. Learn about Glutaric Acidemia Type 2.
- Glycogen Storage Disease Type 0Dr. Breilyn isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Glycogen Storage Disease Type 13Dr. Breilyn isAdvanced. Learn about Glycogen Storage Disease Type 13.
- Glycogen Storage Disease Type 3Dr. Breilyn isAdvanced. Learn about Glycogen Storage Disease Type 3.
- Glycogen Storage Disease Type 7Dr. Breilyn isAdvanced. Learn about Glycogen Storage Disease Type 7.
- Glycogen Storage Disease Type 9Dr. Breilyn isAdvanced. Learn about Glycogen Storage Disease Type 9.
- Hereditary Fructose IntoleranceDr. Breilyn isAdvanced. Learn about Hereditary Fructose Intolerance.
- HyperlysinemiaDr. Breilyn isAdvanced. Learn about Hyperlysinemia.
- Inborn Amino Acid Metabolism Disorder
- Isovaleric AcidemiaDr. Breilyn isAdvanced. Learn about Isovaleric Acidemia.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine DiseaseDr. Breilyn isAdvanced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaDr. Breilyn isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- N-Acetylglutamate Synthase Deficiency
- Ornithine Translocase DeficiencyDr. Breilyn isAdvanced. Learn about Ornithine Translocase Deficiency.
- Phosphoglycerate Kinase DeficiencyDr. Breilyn isAdvanced. Learn about Phosphoglycerate Kinase Deficiency.
- Phosphoglycerate Mutase DeficiencyDr. Breilyn isAdvanced. Learn about Phosphoglycerate Mutase Deficiency.
- Propionic AcidemiaDr. Breilyn isAdvanced. Learn about Propionic Acidemia.
- Tyrosinemia Type 1Dr. Breilyn isAdvanced. Learn about Tyrosinemia Type 1.
- Tyrosinemia Type 2Dr. Breilyn isAdvanced. Learn about Tyrosinemia Type 2.
- Tyrosinemia Type 3Dr. Breilyn isAdvanced. Learn about Tyrosinemia Type 3.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)Dr. Breilyn isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- AlkaptonuriaDr. Breilyn isExperienced. Learn about Alkaptonuria.
- AminoaciduriaDr. Breilyn isExperienced. Learn about Aminoaciduria.
- Aplasia Cutis CongenitaDr. Breilyn isExperienced. Learn about Aplasia Cutis Congenita.
- Autosomal Recessive Congenital Methemoglobinemia
- Cardiofaciocutaneous SyndromeDr. Breilyn isExperienced. Learn about Cardiofaciocutaneous Syndrome.
- Cardiomyopathic LentiginosisDr. Breilyn isExperienced. Learn about Cardiomyopathic Lentiginosis.
- Clouston SyndromeDr. Breilyn isExperienced. Learn about Clouston Syndrome.
- Costello SyndromeDr. Breilyn isExperienced. Learn about Costello Syndrome.
- Delayed GrowthDr. Breilyn isExperienced. Learn about Delayed Growth.
- Dihydrolipoamide Dehydrogenase DeficiencyDr. Breilyn isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Ectodermal DysplasiasDr. Breilyn isExperienced. Learn about Ectodermal Dysplasias.
- Galactose Epimerase DeficiencyDr. Breilyn isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Breilyn isExperienced. Learn about Galactosemia.
- HomocystinuriaDr. Breilyn isExperienced. Learn about Homocystinuria.
- HypotoniaDr. Breilyn isExperienced. Learn about Hypotonia.
- Methylmalonic AcidemiaDr. Breilyn isExperienced. Learn about Methylmalonic Acidemia.
- Methylmalonic Acidemia with Homocystinuria
- Niemann-Pick DiseaseDr. Breilyn isExperienced. Learn about Niemann-Pick Disease.
- Noonan SyndromeDr. Breilyn isExperienced. Learn about Noonan Syndrome.
- PEPCK 1 DeficiencyDr. Breilyn isExperienced. Learn about PEPCK 1 Deficiency.
- Peroxisomal Acyl-CoA Oxidase DeficiencyDr. Breilyn isExperienced. Learn about Peroxisomal Acyl-CoA Oxidase Deficiency.
- Pyruvate Carboxylase DeficiencyDr. Breilyn isExperienced. Learn about Pyruvate Carboxylase Deficiency.
- Pyruvate Decarboxylase DeficiencyDr. Breilyn isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Breilyn isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- RASopathiesDr. Breilyn isExperienced. Learn about RASopathies.
- ReticulohistiocytomaDr. Breilyn isExperienced. Learn about Reticulohistiocytoma.
- SplenomegalyDr. Breilyn isExperienced. Learn about Splenomegaly.
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
- Thymidine Kinase 2 Deficiency (TK2d)Dr. Breilyn isExperienced. Learn about Thymidine Kinase 2 Deficiency (TK2d).