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 Tyrosinemia Type 2. Her top areas of expertise are Glutaric Acidemia Type 1, Hyperlysinemia, Tyrosinemia Type 3, and Tyrosinemia Type 2. 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.
Children's Hospital Pediatric Associates, Inc
Deborah Marsden is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Marsden is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 2. Her top areas of expertise are Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidoses (MPS), Hydrops Fetalis, and Fetal Edema. Dr. Marsden is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Amy Kritzer is a Pediatrics provider in Boston, Massachusetts. Dr. Kritzer is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 2. Her top areas of expertise are Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Smith-Lemli-Opitz Syndrome.
Children's Hospital Pediatric Associates, Inc
Olaf Bodamer is a Medical Genetics provider in Boston, Massachusetts. Dr. Bodamer is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 2. His top areas of expertise are Kabuki Syndrome, Classic Galactosemia, Niemann-Pick Disease, and Microcephaly. Dr. Bodamer 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).