Overview
Jessica Priestley is a Medical Genetics specialist and a Pediatrics provider in Kentwood, Michigan. Dr. Priestley is rated as an Experienced provider by MediFind in the treatment of X-Linked Creatine Deficiency. Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is currently accepting new patients.
Her clinical research consists of co-authoring 12 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
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
Locations
4444 Kalamazoo Ave Se, 200 Corewell Health Medica, Kentwood, MI 49508
35 Michigan St Ne, 3003 Corewell Health Medic, Grand Rapids, MI 49503
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.
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
- Autosomal Recessive Congenital Methemoglobinemia
- Biotinidase DeficiencyDr. Priestley isAdvanced. Learn about Biotinidase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Classic GalactosemiaDr. Priestley isAdvanced. Learn about Classic Galactosemia.
- Danon DiseaseDr. Priestley isAdvanced. Learn about Danon Disease.
- Experienced
- 15q11.2 MicrodeletionDr. Priestley isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Priestley isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Priestley isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Priestley isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Priestley isExperienced. Learn about 47 XYY Syndrome.