The 20 Best EEC Syndrome Doctors Near Me in Ann Arbor, MI

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 EEC 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.

My clinical practice concentrates on complex pediatric airway, hearing & language development, and care of the child with a congenital syndrome. Dr. Green is rated as an Experienced provider by MediFind in the treatment of EEC Syndrome. He is also highly rated in 32 other conditions, according to our data. His clinical expertise encompasses Tracheobronchomalacia, Acquired Tracheomalacia, CHARGE Syndrome, Adenoidectomy, and Myringotomy. Dr. Green is board certified in Otolaryngology-Head & Neck Surgery.

Mark Hannibal is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Hannibal is rated as an Experienced provider by MediFind in the treatment of EEC 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.

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 EEC 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.

Christian J. Vercler, M.D. is a faculty member in the Section of Plastic Surgery in the Department of Surgery with a joint appointment in the Department of Neurosurgery at Michigan Medicine. He serves as Co-Chief of the Clinical Ethics Service of the Center for Bioethics and Social Sciences in Medicine at the University of Michigan. He is a diplomate of both the American Board of Surgery and the American Board of Plastic Surgery.Dr. Vercler received his Bachelor of Science in Biology and Master of Arts in Theological Studies from Wheaton College (IL). He attended medical school at the University of Illinois College of Medicine. He completed general surgery training at Emory University and plastic surgery at the Harvard Plastic Surgery Program. He then did an additional fellowship in Craniofacial Surgery at the University of Michigan.Dr. Vercler has a special interest in medical ethics. He completed a Fellowship in Clinical Ethics at the Emory University Center for Ethics and earned a Masters of Arts degree in Bioethics from Trinity. He currently serves as the Chair of the Pediatric Ethics Committee of C.S. Mott Children’s Hospital and is Co-Chair of the Adult Ethics Committee at Michigan Medicine. Additionally, he is chair of the Bioethics Committee of the Michigan State Medical Society and past chair of both the ASPS Ethics Committee and Ethics Interest Group of the American Cleft Palate-Craniofacial Association.Clinical Specialization:Dr. Vercler focuses primarily on pediatric plastic surgery and craniofacial deformities in children and adults. Dr. Vercler is rated as an Experienced provider by MediFind in the treatment of EEC Syndrome. He is also highly rated in 47 other conditions, according to our data. His clinical expertise encompasses Metopic Ridge, Craniosynostosis, Plagiocephaly, Bone Graft, and Osteotomy. Dr. Vercler is board certified in Surgery and Plastic Surgery.

Dr. Edwards is the James Hayward Endowed Clinical Professor of Oral & Maxillofacial Surgery and the Chief of Pediatric Oral and Maxillofacial Surgery, and Chair of Oral and Maxillofacial Surgery/Hospital Dentistry. He also serves as the chief of Pediatric Oral and Maxillofacial Surgery at C.S. Mott Children's Hospital. He graduated from the Dalhousie University School of Dentistry and the University of Michigan Medical School. Dr. Edwards completed his residency at the University of Michigan in Oral and Maxillofacial Surgery. After his residency, Dr. Edwards completed fellowship training at the University of Pittsburgh in Craniofacial Surgery and the University of Michigan in Oncology and Microvascular Reconstruction. Dr. Edwards' clinical interests include cleft lip and palate and craniofacial differences and pediatric head and neck oncology and survivorship. Dr. Edwards is rated as an Experienced provider by MediFind in the treatment of EEC Syndrome. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Osteochondroma, Cherubism, Prognathism, Osteotomy, and Myringotomy.

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 EEC Syndrome. 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 EEC 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 EEC 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.