Overview
Billur Moghaddam is a Medical Genetics specialist and a Pediatrics provider in Roseville, California. Dr. Moghaddam is rated as an Experienced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). Her top areas of expertise are Molybdenum Cofactor Deficiency (MoCD), Ehlers-Danlos Syndrome (EDS), Glycogen Storage Disease Type 3, and Dihydropteridine Reductase Deficiency.
Her clinical research consists of co-authoring 4 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
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
Locations
1600 Eureka Rd, Roseville, CA 95661
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.
Katherine Rauen is a Medical Genetics specialist and a Pediatrics provider in Sacramento, California. Dr. Rauen is rated as a Distinguished provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). Her top areas of expertise are RASopathies, Costello Syndrome, Legius Syndrome, and Cardiofaciocutaneous Syndrome.
Sacramento Medical Center
Kamer Tezcan is a Medical Genetics specialist and a Pediatrics provider in Sacramento, California. Dr. Tezcan is rated as an Advanced provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). Her top areas of expertise are Chromosome 10q Deletion, Neurofibromatosis Type 1 (NF1), Chromosome 13q Duplication, and Neurofibromatosis. Dr. Tezcan is currently accepting new patients.
Regents Of The Univ Of Ca
Suma Shankar is a Medical Genetics specialist and an Ophthalmologist in Sacramento, California. Dr. Shankar is rated as a Distinguished provider by MediFind in the treatment of Neurofibromatosis Type 1 (NF1). Her top areas of expertise are Gaucher Disease Type 1, RASopathies, Costello Syndrome, and Fabry Disease.
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
- Ehlers-Danlos Syndrome (EDS)Dr. Moghaddam isAdvanced. Learn about Ehlers-Danlos Syndrome (EDS).
- Molybdenum Cofactor Deficiency (MoCD)Dr. Moghaddam isAdvanced. Learn about Molybdenum Cofactor Deficiency (MoCD).
- Experienced
- 2q37 Deletion SyndromeDr. Moghaddam isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Moghaddam isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Moghaddam isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Moghaddam isExperienced. Learn about Abruzzo-Erickson Syndrome.
- AchondroplasiaDr. Moghaddam isExperienced. Learn about Achondroplasia.
- Acrodermatitis EnteropathicaDr. Moghaddam isExperienced. Learn about Acrodermatitis Enteropathica.