Overview
Cheryl Garganta is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Garganta is highly rated in 6 conditions, according to our data. Her top areas of expertise are Hyperlysinemia, Glutaric Acidemia Type 1, Tyrosinemia Type 2, and Tyrosinemia Type 3. 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.
Specialties
Licenses
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
- 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.
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Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow is highly rated in 159 conditions, according to our data. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow is currently accepting new patients.
Frequently Asked Questions about Dr. Cheryl L. Garganta
How do I make an appointment with Dr. Cheryl L. Garganta?
You can book an appointment with Dr. Cheryl L. Garganta by calling their office at 617-636-5000. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Cheryl L. Garganta a top-rated expert for Hyperlysinemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Cheryl L. Garganta is classified as an Advanced expert for Hyperlysinemia, 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. Cheryl L. Garganta specialize in?
While Dr. Cheryl L. Garganta is a Medical Genetics, they have specific expertise in Hyperlysinemia, Glutaric Acidemia Type 1, and Tyrosinemia Type 2. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Cheryl L. Garganta participate in research or clinical trials?
Yes. Dr. Cheryl L. Garganta has published 10 articles and abstracts on conditions like Hyperlysinemia. You can view a list of Dr. Cheryl L. Garganta's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Cheryl L. Garganta accept my insurance?
Dr. Cheryl L. Garganta accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 617-636-5000 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
- 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).