Overview
Willa Thorson is a Medical Genetics specialist and a Pediatrics provider in Miami, Florida. Dr. Thorson is rated as an Experienced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are CHARGE Syndrome, Classic Galactosemia, KBG Syndrome, and Galactosemia. Dr. Thorson is currently accepting new patients.
Her clinical research consists of co-authoring 16 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 Galactose Epimerase Deficiency.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER MEDICARE PART D
- EPO
- HMO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
1611 Nw 12 Th Ave, Jackson Memorial Hospital, Miami, FL 33136
1601 Nw 12th Ave, Miami, FL 33136
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.
University Of Miami
Kumarie Latchman is a Medical Genetics provider in Miami, Florida. Dr. Latchman is rated as an Experienced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Classic Galactosemia, Early Infantile Epileptic Encephalopathy, Choanal Atresia, and Galactose Epimerase Deficiency. Dr. Latchman is currently accepting new patients.
University Of Miami
Deborah Barbouth is a Medical Genetics specialist and a Pediatrics provider in Miami, Florida. Dr. Barbouth is rated as an Advanced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Gaucher Disease Type 1, Gaucher Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Splenectomy. Dr. Barbouth is currently accepting new patients.
Guney Bademci is a Medical Genetics provider in Miami, Florida. Dr. Bademci is rated as a Distinguished provider by MediFind in the treatment of Galactose Epimerase Deficiency. His top areas of expertise are Branchiootorenal Syndrome, Branchio-Oculo-Facial Syndrome (BOFS), KBG Syndrome, and RASopathies. Dr. Bademci is currently accepting new patients.
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
- CHARGE SyndromeDr. Thorson isAdvanced. Learn about CHARGE Syndrome.
- Classic GalactosemiaDr. Thorson isAdvanced. Learn about Classic Galactosemia.
- KBG SyndromeDr. Thorson isAdvanced. Learn about KBG Syndrome.
- Experienced
- 15q11.2 MicrodeletionDr. Thorson isExperienced. Learn about 15q11.2 Microdeletion.
- 3p Deletion SyndromeDr. Thorson isExperienced. Learn about 3p Deletion Syndrome.
- 46XX Testicular Disorder of Sex Development
- AlbinismDr. Thorson isExperienced. Learn about Albinism.
- Beckwith-Wiedemann SyndromeDr. Thorson isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Beta-Ketothiolase DeficiencyDr. Thorson isExperienced. Learn about Beta-Ketothiolase Deficiency.