The 20 Best Beckwith-Wiedemann Syndrome Doctors Near Me in Michigan, US

Stephanie Campbell is a Pediatrics provider practicing medicine in Royal Oak, Michigan. She has been practicing medicine for over 10 years. Dr. Campbell is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Increased Head Circumference, Delayed Growth, Congenital Athymia, and Acromesomelic Dysplasia Campailla Martinelli Type. Dr. Campbell is board certified in American Board Of Pediatrics. Dr. Campbell 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 Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. 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.

Mark Hannibal is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Hannibal is rated as an Advanced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 166 other conditions, according to our data. His clinical expertise encompasses Aase Syndrome, CHARGE Syndrome, Cockayne Syndrome Type 2, and Hennekam Syndrome. Dr. Hannibal is board certified in 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 Advanced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. 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.

Timothy Moss is a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Moss is rated as an Advanced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Simpson-Golabi-Behmel Syndrome, Megalencephaly-Capillary Malformation Syndrome, Beckwith-Wiedemann Syndrome, and Perlman Syndrome.

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 Beckwith-Wiedemann Syndrome. 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.

Cooking, spending time with my family. Dr. Ames is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. 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.

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 Beckwith-Wiedemann Syndrome. 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.

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 Beckwith-Wiedemann Syndrome. 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.

Vinod Misra is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Detroit, Michigan. Dr. Misra is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Micrognathia, Osteogenesis Imperfecta, Microcephaly, and Mixed Gonadal Dysgenesis.

Leigh Flore is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Detroit, Michigan. Dr. Flore is rated as an Experienced provider by MediFind in the treatment of Beckwith-Wiedemann Syndrome. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Simpson-Golabi-Behmel Syndrome, Pyruvate Carboxylase Deficiency, Cantu Syndrome, and Proteus-Like Syndrome.

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 Beckwith-Wiedemann Syndrome. 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.