Overview
Mary-alice Abbott is a Medical Genetics specialist and a Pediatrics provider in Springfield, Massachusetts. Dr. Abbott is highly rated in 8 conditions, according to our data. Her top areas of expertise are Pompe Disease, Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Danon Disease, and Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome).
Her clinical research consists of co-authoring 22 peer reviewed articles and participating in 1 clinical trial. 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
- PPO
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
Locations
50 Wason Ave, Springfield, MA 01107
280 Chestnut St, Suite 2, Springfield, MA 01199
55 Lake Ave N, Worcester, MA 01655
Additional Areas of Focus
Dr. Abbott has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
1 Clinical Trials
Gabriel Cohn is a Medical Genetics provider in Springfield, Massachusetts. Dr. Cohn is highly rated in 2 conditions, according to our data. His top areas of expertise are Gaucher Disease Type 1, Gaucher Disease, and Farber Lipogranulomatosis.
Yale University
Yong-hui Jiang is a Medical Genetics specialist and a Pediatrics provider in New Haven, Connecticut. Dr. Jiang is highly rated in 6 conditions, according to our data. His top areas of expertise are Angelman Syndrome, Autism Spectrum Disorder, MELAS Syndrome, and Prader-Willi Syndrome.
Peter Benn is a Medical Genetics provider in Farmington, Connecticut. Dr. Benn is highly rated in 7 conditions, according to our data. His top areas of expertise are Trisomy 13, Chromosome 13q Duplication, Mosaicism, and Trisomy 18.
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
- Pompe DiseaseDr. Abbott isDistinguished. Learn about Pompe Disease.
- Advanced
- Danon DiseaseDr. Abbott isAdvanced. Learn about Danon Disease.
- Mucopolysaccharidoses (MPS)Dr. Abbott isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A)
- N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
- Experienced
- 15q11.2 MicrodeletionDr. Abbott isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Abbott isExperienced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Abbott isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Abbott isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Abbott isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Abbott isExperienced. Learn about Aase Syndrome.