The 20 Best Phenylketonuria (PKU) Doctors Near Me in Michigan, US

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 Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). 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.

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 Phenylketonuria (PKU). 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.

Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Quinonez is rated as an Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). 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. 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 Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). 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.

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 Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). 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.

Kara Pappas is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Detroit, Michigan. Dr. Pappas is rated as an Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). 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.

Stacie Adams is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Grand Rapids, Michigan. Dr. Adams is rated as an Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). 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.

Cooking, spending time with my family. Dr. Ames is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Cardiomyopathic Lentiginosis, Cardiofaciocutaneous Syndrome, and Noonan Syndrome. Dr. Ames is board certified in Pediatrics, Clinical Genetics & Genomics, and Medical Biochemical Genetics.

Tomoyasu Higashimoto is a Medical Genetics specialist and an Internal Medicine provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). 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. Toma earned his medical degree from Baghdad University (2001) and completed a Master’s of Public Health from the University of Albany (2007). He completed his residency training in Family Medicine at Beaumont Hospital (2011) and also a fellowship training in Geriatric Medicine at the University of Michigan (2012).He is passionate about chronic diseases management, preventive medicine and complex care. Dr. Toma is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). He is also highly rated in 6 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Vertigo, Maturity Onset Diabetes of the Young, Ureteroscopy, and Endoscopy.

Dr. Soyster is a graduate of U-M Medical School and completed her internal medicine residency at Henry Ford Hospital. Dr. Soyster is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Juvenile Primary Osteoporosis, Familial Hypertension, Glucocorticoid-Remediable Aldosteronism, and Hypertension.

Sidhartha Tan is a Neonatologist and a Pediatrics provider practicing medicine in Detroit, Michigan. Dr. Tan is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Cerebral Hypoxia, Spastic Diplegia Infantile Type, Asphyxia Neonatorum, and Placental Insufficiency.

David Stockton is a primary care provider, practicing in Internal Medicine in Detroit, Michigan. Dr. Stockton is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). He is also highly rated in 6 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Danon Disease, Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.

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 Phenylketonuria (PKU). 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.

Anthony Songco is a primary care provider, practicing in Family Medicine in Monroe, Michigan. Dr. Songco is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Lung Metastases, Boils, Glucocorticoid-Remediable Aldosteronism, and Hypertension.

Natalie Parr is a primary care provider, practicing in Internal Medicine in Wyoming, Michigan. Dr. Parr is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Type 2 Diabetes (T2D), Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, and Hypertension.

Robert Mackie is a primary care provider, practicing in Family Medicine in Sault Sainte Marie, Michigan. Dr. Mackie is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Migraine, Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), Hip Replacement, and Ureteroscopy.

Noelle Fabie is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Detroit, Michigan. Dr. Fabie is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Micrognathia, Trichorhinophalangeal Syndrome Type 2, CHARGE Syndrome, and Scalp-Ear-Nipple Syndrome. Dr. Fabie is currently accepting new patients.

Lory Read is a primary care provider, practicing in Family Medicine in Lakeview, Michigan. Dr. Read is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). She is also highly rated in 15 other conditions, according to our data. Her clinical expertise encompasses Seasonal Affective Disorder (SAD), Atherosclerosis, Coronary Heart Disease, and End-Stage Renal Disease (ESRD).

Thomas Teal is a primary care provider, practicing in Family Medicine in Owosso, Michigan. Dr. Teal is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Sarcoidosis, Neurosarcoidosis, Mccune-Albright Syndrome, and Chronic Cough.