Overview
Wendy Smith is a Medical Genetics specialist and a Pediatrics provider in Portland, Maine. Dr. Smith is rated as an Advanced provider by MediFind in the treatment of Dihydropteridine Reductase Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Urea Cycle Disorders (UCD), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.
Her clinical research consists of co-authoring 32 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
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- MANAGED MEDICAID PLAN
- EPO
- HMO
- POS
- PPO
- MEDICARE DISCOUNT CARD
- MEDICARE PDP
- OTHER MEDICARE
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
22 Bramhall St, Portland, ME 04102
1577 Congress St, Portland, ME 04102
Additional Areas of Focus
Dr. Smith 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
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
- Phenylketonuria (PKU)Dr. Smith isDistinguished. Learn about Phenylketonuria (PKU).
- Urea Cycle Disorders (UCD)Dr. Smith isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Chromosome 13q DeletionDr. Smith isAdvanced. Learn about Chromosome 13q Deletion.
- Danon DiseaseDr. Smith isAdvanced. Learn about Danon Disease.
- Dihydropteridine Reductase Deficiency
- Fabry DiseaseDr. Smith isAdvanced. Learn about Fabry Disease.
- Galactokinase DeficiencyDr. Smith isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Smith isAdvanced. Learn about Galactose Epimerase Deficiency.
- Experienced
- 15q11.2 MicrodeletionDr. Smith isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Smith isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Smith isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Smith isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Smith isExperienced. Learn about 47 XYY Syndrome.