The 20 Best Hyperlysinemia Doctors Near Me in Michigan, US

Carrie Kastein is a Pediatrics provider practicing medicine in Zeeland, Michigan. She has been practicing medicine for over 10 years. Dr. Kastein is rated as an Experienced provider by MediFind in the treatment of Hyperlysinemia. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Obesity in Children, Hyperlysinemia, Autism Spectrum Disorder, and Developmental Dysphasia Familial. Dr. Kastein is board certified in American Board Of Pediatrics.

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 Hyperlysinemia. 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 Hyperlysinemia. 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.

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 Hyperlysinemia. 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.

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 Hyperlysinemia. 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.

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 Hyperlysinemia. 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.

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

Allison Bannick is a Nurse Practitioner practicing medicine in Grand Rapids, Michigan. Bannick, NP is rated as an Experienced provider by MediFind in the treatment of Hyperlysinemia. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Activated PI3K Delta Syndrome (APDS), Hyperlysinemia, and Urea Cycle Disorders (UCD).

Ria Garg is a Medical Genetics provider practicing medicine in Detroit, Michigan. Dr. Garg is rated as an Experienced provider by MediFind in the treatment of Hyperlysinemia. Her clinical expertise encompasses Chromosome 8p Deletion, Chromosome 6q Duplication, Currarino Triad, and Abruzzo-Erickson Syndrome.

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 Hyperlysinemia. 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 Hyperlysinemia. 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.

Curtis Hunt is a primary care provider, practicing in Internal Medicine in Troy, Michigan. Dr. Hunt is rated as an Experienced provider by MediFind in the treatment of Hyperlysinemia. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Familial Hypertriglyceridemia, Blood Clots, Gout, and Hyperlysinemia.