Overview
Amy Kritzer is a Pediatrics provider practicing medicine in Boston, Massachusetts.
Dr. Kritzer is highly rated in 12 conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B), Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A), and Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome).
Dr. Kritzer is board certified in Pediatrics, Clinical Genetics And Genomics, and Medical Biochemical Genetics. She is actively involved in clinical research, co-authoring 31 peer reviewed articles and participating in 1 clinical trial. Dr. Kritzer is currently accepting new patients.
Specialties
Licenses
Board Certifications
Fellowships
Hospital Affiliations
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
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- HMO
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- PPO
- EPO
- MANAGED MEDICAID PLAN
- HMO
- EPO
- HMO
- POS
- PPO
Locations
300 Longwood Ave, Boston, MA 02115
1 Medical Ctr Dr, Lebanon, NH 03756
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
Fowzan Alkuraya is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Boston, Massachusetts. Dr. Alkuraya is highly rated in 72 conditions, according to our data. His clinical expertise encompasses Achalasia Microcephaly Syndrome, Microcephaly, Early Infantile Epileptic Encephalopathy, Cortical Dysplasia, and Vitrectomy.
The Dialysis Center At Waltham
Kenneth Huttner is a Pediatrics provider practicing medicine in Waltham, Massachusetts. Dr. Huttner is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Clouston Syndrome, Aplasia Cutis Congenita, and Ectodermal Dysplasias.
Massachusetts General Hospital
Katharine Zuckerman is a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Zuckerman is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Autism Spectrum Disorder. Dr. Zuckerman is currently accepting new patients.
Frequently Asked Questions about Dr. Amy M. Kritzer
How do I make an appointment with Dr. Amy M. Kritzer?
You can book an appointment with Dr. Amy M. Kritzer by calling their office at 617-355-6000. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Amy M. Kritzer a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Amy M. Kritzer is classified as an Distinguished expert for Phenylketonuria (PKU), 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. Amy M. Kritzer specialize in?
While Dr. Amy M. Kritzer is a Pediatrics, they have specific expertise in Phenylketonuria (PKU), Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B), and Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Amy M. Kritzer participate in research or clinical trials?
Yes. Dr. Amy M. Kritzer has published 31 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Dr. Amy M. Kritzer's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Amy M. Kritzer accept my insurance?
Dr. Amy M. Kritzer accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 617-355-6000 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
- Distinguished
- Phenylketonuria (PKU)Dr. Kritzer isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Fabry DiseaseDr. Kritzer isAdvanced. Learn about Fabry Disease.
- Glutaric Acidemia Type 2Dr. Kritzer isAdvanced. Learn about Glutaric Acidemia Type 2.
- HyperlysinemiaDr. Kritzer isAdvanced. Learn about Hyperlysinemia.
- Mucopolysaccharidoses (MPS)Dr. Kritzer isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Urea Cycle Disorders (UCD)Dr. Kritzer isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Von Gierke DiseaseDr. Kritzer isAdvanced. Learn about Von Gierke Disease.
- Experienced
- 15q11.2 MicrodeletionDr. Kritzer isExperienced. Learn about 15q11.2 Microdeletion.
- Absence of TibiaDr. Kritzer isExperienced. Learn about Absence of Tibia.
- Acid Sphingomyelinase Deficiency (ASMD)Dr. Kritzer isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Activated PI3K Delta Syndrome (APDS)Dr. Kritzer isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Alpha MannosidosisDr. Kritzer isExperienced. Learn about Alpha Mannosidosis.
- AminoaciduriaDr. Kritzer isExperienced. Learn about Aminoaciduria.
- Arthrogryposis Multiplex CongenitaDr. Kritzer isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- AspartylglucosaminuriaDr. Kritzer isExperienced. Learn about Aspartylglucosaminuria.
- Atelosteogenesis Type 2Dr. Kritzer isExperienced. Learn about Atelosteogenesis Type 2.
- Autism Spectrum DisorderDr. Kritzer isExperienced. Learn about Autism Spectrum Disorder.
- Autosomal Recessive Congenital Methemoglobinemia
- Beta-Ketothiolase DeficiencyDr. Kritzer isExperienced. Learn about Beta-Ketothiolase Deficiency.
- Beta-MannosidosisDr. Kritzer isExperienced. Learn about Beta-Mannosidosis.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- CHARGE SyndromeDr. Kritzer isExperienced. Learn about CHARGE Syndrome.
- Childhood PancreatitisDr. Kritzer isExperienced. Learn about Childhood Pancreatitis.
- Congenital AthymiaDr. Kritzer isExperienced. Learn about Congenital Athymia.
- Delayed GrowthDr. Kritzer isExperienced. Learn about Delayed Growth.
- Diastrophic DysplasiaDr. Kritzer isExperienced. Learn about Diastrophic Dysplasia.
- Dihydrolipoamide Dehydrogenase DeficiencyDr. Kritzer isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Distal 18q Deletion SyndromeDr. Kritzer isExperienced. Learn about Distal 18q Deletion Syndrome.
- Early Infantile Epileptic EncephalopathyDr. Kritzer isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- FucosidosisDr. Kritzer isExperienced. Learn about Fucosidosis.
- Gaucher DiseaseDr. Kritzer isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Kritzer isExperienced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Kritzer isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Kritzer isExperienced. Learn about Gaucher Disease Type 3.
- HNRNPH2-Related DisorderDr. Kritzer isExperienced. Learn about HNRNPH2-Related Disorder.
- HypotoniaDr. Kritzer isExperienced. Learn about Hypotonia.
- Infantile NeutropeniaDr. Kritzer isExperienced. Learn about Infantile Neutropenia.
- Jacobsen SyndromeDr. Kritzer isExperienced. Learn about Jacobsen Syndrome.
- JaundiceDr. Kritzer isExperienced. Learn about Jaundice.
- Koolen De Vries SyndromeDr. Kritzer isExperienced. Learn about Koolen De Vries Syndrome.
- Microcephaly Deafness SyndromeDr. Kritzer isExperienced. Learn about Microcephaly Deafness Syndrome.
- Newborn JaundiceDr. Kritzer isExperienced. Learn about Newborn Jaundice.
- Niemann-Pick DiseaseDr. Kritzer isExperienced. Learn about Niemann-Pick Disease.
- PEPCK 1 DeficiencyDr. Kritzer isExperienced. Learn about PEPCK 1 Deficiency.
- Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy
- Pompe DiseaseDr. Kritzer isExperienced. Learn about Pompe Disease.
- Pyruvate Carboxylase DeficiencyDr. Kritzer isExperienced. Learn about Pyruvate Carboxylase Deficiency.
- Schindler DiseaseDr. Kritzer isExperienced. Learn about Schindler Disease.
- Short Stature (Growth Disorders)Dr. Kritzer isExperienced. Learn about Short Stature (Growth Disorders).
- Wildervanck SyndromeDr. Kritzer isExperienced. Learn about Wildervanck Syndrome.