MediFind found 5 doctor with experience in Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency near Grand Rapids, MI. Of these, 3 are Experienced and 2 are Advanced.
Spectrum Health Hospitals
Laurie Seaver is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Seaver is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Hypotonia, 1p36 Deletion Syndrome, Smith-Magenis Syndrome, and Potocki-Lupski Syndrome. Dr. Seaver is currently accepting new patients.
Robert Conway is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Conway is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Hypermethioninemia, Biotinidase Deficiency, Phenylketonuria (PKU), and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Conway is currently accepting new patients.
Spectrum Health Primary Care Partners
Stanley Sedore is a Pediatric Cardiologist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Sedore is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Familial Dilated Cardiomyopathy, Brugada Syndrome, Postural Orthostatic Tachycardia Syndrome (POTS), and Short QT Syndrome.
Stacie Adams is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Adams is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactosemia. Dr. Adams is currently accepting new patients.
Spectrum Health Primary Care Partners
Jessica Priestley is a Medical Genetics specialist and a Pediatrics provider in Kentwood, Michigan. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) 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.
Last Updated: 10/30/2025