Overview
Sihoun Hahn is a Medical Genetics specialist and a Pediatrics provider in Seattle, Washington. Dr. Hahn is rated as an Experienced provider by MediFind in the treatment of Chromosome 6 Uniparental Disomy. His top areas of expertise are Wilson Disease, Menkes Disease, Carnitine-Acylcarnitine Translocase Deficiency, and Pompe Disease. Dr. Hahn is currently accepting new patients.
His clinical research consists of co-authoring 6 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
- PPO
- PPO
- EPO
- PPO
- INSURANCE PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- PPO
- EPO
- HMO
- POS
- PPO
Locations
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
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 6 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 6 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 6 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
- Distinguished
- Wilson DiseaseDr. Hahn isDistinguished. Learn about Wilson Disease.
- Advanced
- Carnitine-Acylcarnitine Translocase Deficiency
- Menkes DiseaseDr. Hahn isAdvanced. Learn about Menkes Disease.
- Experienced
- Chromosome 6 Uniparental DisomyDr. Hahn isExperienced. Learn about Chromosome 6 Uniparental Disomy.
- Pompe DiseaseDr. Hahn isExperienced. Learn about Pompe Disease.