Overview
Anne O'donnell-Luria is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. O'donnell-Luria is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). Her top areas of expertise are Chromosome 2 Uniparental Disomy, Chromosome 6 Uniparental Disomy, Chromosome 11 Uniparental Disomy, and Pallister-Killian Mosaic Syndrome. Dr. O'donnell-Luria is currently accepting new patients.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
Locations
Harvey Levy is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Levy is rated as a Distinguished provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Phenylketonuria (PKU), Homocystinuria, Maternal Hyperphenylalaninemia, and Classic Galactosemia. Dr. Levy is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow is rated as a Distinguished provider by MediFind in the treatment of Phenylketonuria (PKU). Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow 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 Phenylketonuria (PKU). Her top areas of expertise are Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A).
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
- Chromosome 11 Uniparental DisomyDr. O'donnell-Luria isAdvanced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 2 Uniparental DisomyDr. O'donnell-Luria isAdvanced. Learn about Chromosome 2 Uniparental Disomy.
- Chromosome 6 Uniparental DisomyDr. O'donnell-Luria isAdvanced. Learn about Chromosome 6 Uniparental Disomy.
- Glutaric Acidemia Type 2Dr. O'donnell-Luria isAdvanced. Learn about Glutaric Acidemia Type 2.
- Mosaic Variegated Aneuploidy SyndromeDr. O'donnell-Luria isAdvanced. Learn about Mosaic Variegated Aneuploidy Syndrome.
- Pallister-Killian Mosaic SyndromeDr. O'donnell-Luria isAdvanced. Learn about Pallister-Killian Mosaic Syndrome.
- Experienced
- 2q37 Deletion SyndromeDr. O'donnell-Luria isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyDr. O'donnell-Luria isExperienced. Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
- 3MC SyndromeDr. O'donnell-Luria isExperienced. Learn about 3MC Syndrome.
- 47 XYY SyndromeDr. O'donnell-Luria isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. O'donnell-Luria isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. O'donnell-Luria isExperienced. Learn about Abruzzo-Erickson Syndrome.