Overview
Stacie Adams is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Grand Rapids, Michigan.
Dr. Adams is highly rated in 20 conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactose Epimerase Deficiency.
She is actively involved in clinical research, co-authoring 7 peer reviewed articles. Dr. Adams is currently accepting new patients.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- 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
- POS
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- 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
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.
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Frequently Asked Questions about Dr. Stacie D. Adams
How do I make an appointment with Dr. Stacie D. Adams?
You can book an appointment with Dr. Stacie D. Adams by calling their office at 616-486-9830. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Stacie D. Adams a top-rated expert for Propionic Acidemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Stacie D. Adams is classified as an Advanced expert for Propionic Acidemia, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Stacie D. Adams specialize in?
While Dr. Stacie D. Adams is a Medical Genetics, they have specific expertise in Propionic Acidemia, Classic Galactosemia, and Biotinidase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Stacie D. Adams participate in research or clinical trials?
Yes. Dr. Stacie D. Adams has published 7 articles and abstracts on conditions like Propionic Acidemia. You can view a list of Dr. Stacie D. Adams's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Stacie D. Adams accept my insurance?
Dr. Stacie D. Adams accepts most major insurance plans, including Blue Cross Blue Shield and Humana. We recommend calling the office directly at 616-486-9830 to verify that your specific plan is currently accepted before your visit.
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
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Argininosuccinic AciduriaDr. Adams isAdvanced. Learn about Argininosuccinic Aciduria.
- Biotinidase DeficiencyDr. Adams isAdvanced. Learn about Biotinidase Deficiency.
- Classic GalactosemiaDr. Adams isAdvanced. Learn about Classic Galactosemia.
- Danon DiseaseDr. Adams isAdvanced. Learn about Danon Disease.
- Dihydropteridine Reductase Deficiency
- Fabry DiseaseDr. Adams isAdvanced. Learn about Fabry Disease.
- Galactose Epimerase DeficiencyDr. Adams isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Adams isAdvanced. Learn about Galactosemia.
- Maternal HyperphenylalaninemiaDr. Adams isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Mucopolysaccharidoses (MPS)Dr. Adams isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple Sulfatase DeficiencyDr. Adams isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Ornithine Transcarbamylase Deficiency
- Ornithine Translocase Deficiency
- Phenylketonuria (PKU)Dr. Adams isAdvanced. Learn about Phenylketonuria (PKU).
- Pompe DiseaseDr. Adams isAdvanced. Learn about Pompe Disease.
- Propionic AcidemiaDr. Adams isAdvanced. Learn about Propionic Acidemia.
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Adams isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Adrenoleukodystrophy (ALD)Dr. Adams isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Autosomal Recessive Congenital Methemoglobinemia
- Beta-Ketothiolase DeficiencyDr. Adams isExperienced. Learn about Beta-Ketothiolase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Galactokinase DeficiencyDr. Adams isExperienced. Learn about Galactokinase Deficiency.
- Gaucher DiseaseDr. Adams isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Adams isExperienced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Adams isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Adams isExperienced. Learn about Gaucher Disease Type 3.
- Glycine EncephalopathyDr. Adams isExperienced. Learn about Glycine Encephalopathy.
- Glycogen Storage Disease Type 3Dr. Adams isExperienced. Learn about Glycogen Storage Disease Type 3.
- HypotoniaDr. Adams isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Adams isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- MELAS SyndromeDr. Adams isExperienced. Learn about MELAS Syndrome.
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Newborn JaundiceDr. Adams isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarDr. Adams isExperienced. Learn about Newborn Low Blood Sugar.
- PEPCK 1 DeficiencyDr. Adams isExperienced. Learn about PEPCK 1 Deficiency.
- Protein DeficiencyDr. Adams isExperienced. Learn about Protein Deficiency.
- Pyruvate Carboxylase DeficiencyDr. Adams isExperienced. Learn about Pyruvate Carboxylase Deficiency.
- Pyruvate Decarboxylase DeficiencyDr. Adams isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Adams isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- Thymidine Kinase 2 Deficiency (TK2d)Dr. Adams isExperienced. Learn about Thymidine Kinase 2 Deficiency (TK2d).
- Urea Cycle Disorders (UCD)Dr. Adams isExperienced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Von Gierke DiseaseDr. Adams isExperienced. Learn about Von Gierke Disease.


