Overview
Cheryl Garganta is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Garganta is rated as an Advanced provider by MediFind in the treatment of Hyperlysinemia. Her top areas of expertise are Hyperlysinemia, Glutaric Acidemia Type 1, Tyrosinemia Type 3, and Tyrosinemia Type 1. Dr. Garganta is currently accepting new patients.
Her clinical research consists of co-authoring 10 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
- EPO
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- EPO
- HMO
- POS
- 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.
Tracy Mcgregor is a Medical Genetics specialist and a Pediatrics provider in Cambridge, Massachusetts. Dr. Mcgregor is rated as an Advanced provider by MediFind in the treatment of Hyperlysinemia. Her top areas of expertise are Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Hyperlysinemia, Subglottic Stenosis, and Molybdenum Cofactor Deficiency (MoCD). Dr. Mcgregor is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Amy Kritzer is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Kritzer is rated as a Distinguished provider by MediFind in the treatment of Hyperlysinemia. Her top areas of expertise are Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Smith-Lemli-Opitz Syndrome. Dr. Kritzer is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow is rated as a Distinguished provider by MediFind in the treatment of Hyperlysinemia. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow 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
- Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects
- Glutaric Acidemia Type 1Dr. Garganta isAdvanced. Learn about Glutaric Acidemia Type 1.
- HyperlysinemiaDr. Garganta isAdvanced. Learn about Hyperlysinemia.
- Tyrosinemia Type 1Dr. Garganta isAdvanced. Learn about Tyrosinemia Type 1.
- Tyrosinemia Type 2Dr. Garganta isAdvanced. Learn about Tyrosinemia Type 2.
- Tyrosinemia Type 3Dr. Garganta isAdvanced. Learn about Tyrosinemia Type 3.
- Experienced
- Dandy-Walker SyndromeDr. Garganta isExperienced. Learn about Dandy-Walker Syndrome.
- HypotoniaDr. Garganta isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Garganta isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseDr. Garganta isExperienced. Learn about Maple Syrup Urine Disease.
- Nonbullous Congenital Ichthyosiform Erythroderma
- Phenylketonuria (PKU)Dr. Garganta isExperienced. Learn about Phenylketonuria (PKU).