Dr. Raelynn Forsyth
Overview
RaeLynn Forsyth, MD, specializes in medical genetics as well as pediatric genetics and genomics and is board-certified by the American Board of Pediatrics and the American Board of Medical Genetics and Genomics. She practices at Medical Genetics Metabolic in Lawrenceville, Medical Genetics in Lawrenceville, and Medical Genetics in Erie and is affiliated with UPMC Hamot, UPMC Children's Hospital of Pittsburgh, UPMC Magee-Womens Hospital, and UPMC Presbyterian. Dr. Forsyth completed her medical degree and a fellowship at the University of Pittsburgh School of Medicine in addition to a residency and fellowship at The Johns Hopkins University School of Medicine.
Dr. Forsyth is highly rated in 1 condition, according to our data. Her top areas of expertise are Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Inborn Amino Acid Metabolism Disorder, and Carbamoyl Phosphate Synthetase 1 Deficiency.
Her clinical research consists of co-authoring 3 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
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- MANAGED MEDICAID PLAN
- HMO
- MANAGED MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
Locations
4401 Penn Avenue, Pittsburgh, PA 15224
4401 Penn Avenue, Pittsburgh, PA 15224
118 East 2nd Street, Suite W1150, Erie, PA 16507
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.
University Of Pittsburgh Physicians
Jirair Bedoyan is a Medical Genetics specialist and a Pediatrics provider in Pittsburgh, Pennsylvania. Dr. Bedoyan is highly rated in 5 conditions, according to our data. His top areas of expertise are Pyruvate Dehydrogenase Deficiency, Pyruvate Decarboxylase Deficiency, Dihydrolipoamide Dehydrogenase Deficiency, Urea Cycle Disorders (UCD), and Gastrostomy. Dr. Bedoyan is currently accepting new patients.
University Of Pittsburgh Physicians
Uta Lichter-Konecki is a Pediatrics specialist and a Medical Genetics provider in Pittsburgh, Pennsylvania. Dr. Lichter-Konecki is highly rated in 7 conditions, according to our data. Her top areas of expertise are Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Maple Syrup Urine Disease, and Hypotonia.
Medical Genetics In Lawrenceville
Joshua Owens, MD, specializes in medical genetics in addition to pediatric genetics and genomics and is board-certified by the American Board of Medical Genetics and Genomics. He practices at Medical Genetics in Lawrenceville and Medical Genetics in Sewickley and is affiliated with UPMC Children's Hospital of Pittsburgh, UPMC Magee-Womens Hospital, and UPMC Presbyterian. Dr. Owens received his medical degree from the University of South Carolina School of Medicine and completed his residency at Cincinnati Children's Hospital Medical Center. Dr. Owens is highly rated in 2 conditions, according to our data. His top areas of expertise are Early Infantile Epileptic Encephalopathy, Primary Ciliary Dyskinesia (PCD), Lateral Meningocele Syndrome, and Joubert Syndrome.
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
- Urea Cycle Disorders (UCD)Dr. Forsyth isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Experienced
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Inborn Amino Acid Metabolism DisorderDr. Forsyth isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Mitochondrial Trifunctional Protein Deficiency
- Ornithine Transcarbamylase DeficiencyDr. Forsyth isExperienced. Learn about Ornithine Transcarbamylase Deficiency.