The 20 Best Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency Doctors Near Me in Michigan, US

Ali Khan is a primary care provider, practicing in Internal Medicine in Pigeon, Michigan. Dr. Khan is rated as a Distinguished provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 42 other conditions, according to our data. His clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Coronary Heart Disease, Low Sodium Level, Ringworm, and Hip Replacement. Dr. Khan is currently accepting new patients.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 8 years. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics, American Board Of Medical Genetics And Genomics, and American Board Of Pediatrics.

Laurie Seaver is a Medical Genetics provider practicing medicine 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. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses 1p36 Deletion Syndrome, Hypotonia, Smith-Magenis Syndrome, and Potocki-Lupski Syndrome. Dr. Seaver is currently accepting new patients.

Dr. Meisner is a board-certified pediatric cardiologist and physician scientist. His clinical focus is on cardiovascular genetics, and he provides the pediatric cardiology services in the multidisciplinary hypertrophic cardiomyopathy, muscular dystrophy, cardiovascular genetics and aortopathy, and RASopathy clinics. He also sees general cardiology and molecular and biochemical cardiology patients in his individual clinics. His translational research laboratory utilizes induced pluripotent stem cell cardiomyocyte and innovative mouse models to understand the pathophysiology and clinical course that leads to cardiomyopathy in children and young adults. Dr. Meisner is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 23 other conditions, according to our data. His clinical expertise encompasses CHARGE Syndrome, Noonan Syndrome, Cardiomyopathic Lentiginosis, and Cardiofaciocutaneous Syndrome. Dr. Meisner is board certified in Pediatric Cardiology and Pediatrics.

Mark W.Russell, M.D. is a board certified Pediatric Cardiologist with a busy clinical practice and research program. Dr. Russell provides the Pediatric Cardiology services for the Hypertrophic Cardiomypathy Program and the Multidisciplinary Muscular Dystrophy Clinic. He directs clinical research studies examining the effect of genetic factors on post-operative outcomes and is the site principal investigator for a multicenter, clinical trial evaluating a new potential treatment for protein-losing enteropathy. He is the director of a biorepository for a multicenter clinical trial sponsored by the Pediatric Heart Network and is a member of the Heart Network's panel that oversees the acquisition and study of biologic samples from patients with congenital heart defects. In addition, he directs a busy laboratory that examines the effects of the extracellular environment on the differentiation of immature cells into cardiac myocytes. Dr. Russell is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 105 other conditions, according to our data. His clinical expertise encompasses Hypertrophic Cardiomyopathy (HCM), Cardiomyopathy, Congenital Heart Disease (CHD), Hypoplastic Left Heart Syndrome (HLHS), and Patent Foramen Ovale Repair. Dr. Russell is board certified in Pediatric Cardiology.

Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. She is also highly rated in 50 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics.

Tomoyasu Higashimoto is a Medical Genetics specialist and an Internal Medicine provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 110 other conditions, according to our data. His clinical expertise encompasses Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia. Dr. Higashimoto is board certified in Family Medicine and Clinical Genetics & Genomics.

Dr. Lee earned her M.D. from Ross University School of Medicine in 2013, and completed Pediatric Residency at Ascension St. John Hospital in Grosse Point, MI, where she served as a Chief Pediatric Resident during her final year of residency. She completed Categorical Medical Genetics Residency at the University of Michigan in 2019. Following this she accepted a dual faculty position as a Clinical Lecturer in the Department of Pediatrics and Department of Internal Medicine for one year, before returning to Fellowship in 2020 to complete additional dedicated training in Medical Biochemical Genetics. After completion of Medical Biochemical Genetics Fellowship, she resumed her faculty position as a Clinical Assistant Professor in 2021. She is board certified in Pediatrics, and in Clinical and General Genetics.She has a dual faculty appointment in the Department of Pediatrics and the Department of Internal Medicine. As a faculty member in the Department of Pediatrics, she sees patients in the Pediatric Genetics and Biochemical Genetics Clinics, in addition to the newly created Multidisciplinary Genetics of Hearing Loss Clinic. As a faculty member in the Department of Internal Medicine, she sees patients in the Adult Medical Genetics and Cancer Genetics Clinics, in addition to patients with atypical diabetes and/or lipodystrophy in collaboration with MEND.In addition to her clinical responsibilities, Dr. Lee also enjoys spending time teaching and discussing various aspects of genetics with fellows, pediatric residents, medical students, and genetic counseling students. Dr. Lee is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. She is also highly rated in 138 other conditions, according to our data. Her clinical expertise encompasses Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome. Dr. Lee is board certified in Pediatrics, Clinical Genetics & Genomics, and Medical Biochemical Genetics.

Stanley Sedore is a Pediatric Cardiologist practicing medicine in Traverse City, Michigan. He has been practicing medicine for over 16 years. Dr. Sedore is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Familial Dilated Cardiomyopathy, Brugada Syndrome, Short QT Syndrome, and Postural Orthostatic Tachycardia Syndrome (POTS). Dr. Sedore is board certified in American Board Of Pediatrics, Pediatric Cardiology - 2016 and American Board Of Pediatrics, Pediatrics - 2013.

Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Quinonez is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 129 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Maple Syrup Urine Disease. Dr. Quinonez is board certified in Pediatrics, Clinical Biochemical Genetics, and Clinical Genetics & Genomics.

Dr. Pritchard is a Michigan native who returned to the University of Michigan to join the faculty here in 2019 after completing her pediatrics and genetics residencies and biochemical genetics fellowship. She enjoys care of complex patients with rare genetic diseases. Dr. Pritchard is active in medical education as Program Director for the Medical Biochemical Genetics Fellowship program and Associate Program Director for the Medical Genetics and Genomics training programs.Outside of work, Dr. Pritchard enjoys cooking, reading, hiking, and spending time with her husband and two daughters. Dr. Pritchard is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. She is also highly rated in 149 other conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Cohen Syndrome.

Omar Jameel is a primary care provider, practicing in Internal Medicine in Royal Oak, Michigan. He has been practicing medicine for over 20 years. Dr. Jameel is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Sepsis, Peptic Ulcer, Necrosis, Bone Marrow Aspiration, and Endoscopy. Dr. Jameel is board certified in American Board Of Internal Medicine. Dr. Jameel is currently accepting new patients.

Stacie Adams is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactose Epimerase Deficiency. Dr. Adams is currently accepting new patients.

Christina Sloan is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Sloan is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Chromosome 6q Duplication, Chromosome 8p Deletion, Delayed Growth, and Fragile XE Syndrome. Dr. Sloan is board certified in Medical Biochemical Genetics and Clinical Genetics & Genomics.

Kara Pappas is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Detroit, Michigan. Dr. Pappas is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Galactosemia, Classic Galactosemia, and Galactose Epimerase Deficiency. Dr. Pappas is currently accepting new patients.

Tucker Billups is a primary care provider, practicing in Internal Medicine in Royal Oak, Michigan. He has been practicing medicine for over 8 years. Dr. Billups is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Enlarged Liver, Hypertensive Heart Disease, Pediatric Myocarditis, and Peptic Ulcer. Dr. Billups is board certified in American Board Of Internal Medicine.

Daniel Misra is a primary care provider, practicing in Internal Medicine in Royal Oak, Michigan. Dr. Misra is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH), Low Sodium Level, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Glucocorticoid-Remediable Aldosteronism.