Overview
Anita Beck is a Medical Genetics specialist and a Pediatrics provider in Seattle, Washington. Dr. Beck is rated as an Advanced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. Her top areas of expertise are Arthrogryposis Multiplex Congenita, Congenital Contractures, 1p36 Deletion Syndrome, and Distal Arthrogryposis Type 6.
Her clinical research consists of co-authoring 38 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Chromosome 11 Uniparental Disomy.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- PPO
- EPO
- PPO
Locations
Additional Areas of Focus
Dr. Beck 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.
Ian Glass is a Medical Genetics provider in Seattle, Washington. Dr. Glass is rated as a Distinguished provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. His top areas of expertise are Joubert Syndrome, Hypotonia, Dandy-Walker Syndrome, and Cortical Dysplasia. Dr. Glass is currently accepting new patients.
Margaret Adam is a Medical Genetics specialist and a Pediatrics provider in Seattle, Washington. Dr. Adam is rated as an Advanced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. Her top areas of expertise are Fetal Alcohol Syndrome (FAS), 1p36 Deletion Syndrome, Intersex, and Microcephaly.
Peter Leahy is a Pediatrics specialist and an Oncologist in Seattle, Washington. Dr. Leahy is rated as an Advanced provider by MediFind in the treatment of Chromosome 11 Uniparental Disomy. His top areas of expertise are Maple Syrup Urine Disease, Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Beta-Ketothiolase Deficiency.
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
- 1p36 Deletion SyndromeDr. Beck isAdvanced. Learn about 1p36 Deletion Syndrome.
- Arthrogryposis Multiplex Congenita
- Chromosome 11 Uniparental Disomy
- Congenital ContracturesDr. Beck isAdvanced. Learn about Congenital Contractures.
- Distal ArthrogryposisDr. Beck isAdvanced. Learn about Distal Arthrogryposis.
- Distal Arthrogryposis Type 6Dr. Beck isAdvanced. Learn about Distal Arthrogryposis Type 6.
- Experienced
- Angelman SyndromeDr. Beck isExperienced. Learn about Angelman Syndrome.
- Beckwith-Wiedemann SyndromeDr. Beck isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Crouzon SyndromeDr. Beck isExperienced. Learn about Crouzon Syndrome.
- HypotoniaDr. Beck isExperienced. Learn about Hypotonia.
- MacroglossiaDr. Beck isExperienced. Learn about Macroglossia.
- MosaicismDr. Beck isExperienced. Learn about Mosaicism.