The 20 Best Dihydrolipoamide Dehydrogenase Deficiency Doctors Near Me in Ann Arbor, MI
Find the Top Dihydrolipoamide Dehydrogenase Deficiency Experts and Specialists
C. S. Mott Children's Hospital
Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Quinonez is rated as a Distinguished provider by MediFind in the treatment of Dihydrolipoamide Dehydrogenase 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.
C. S. Mott Children's Hospital
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 Dihydrolipoamide Dehydrogenase 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.
U Of M Neurology
Steven Leber is a Pediatrics specialist and a Pediatric Neurologist practicing medicine in Ann Arbor, Michigan. Dr. Leber is rated as an Advanced provider by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses Myoclonic Epilepsy, Seizures, Partial Seizure, and Dihydrolipoamide Dehydrogenase Deficiency.
C. S. Mott Children's Hospital
Julie Ziobro is a Pediatrics specialist and a Pediatric Neurologist practicing medicine in Ann Arbor, Michigan. Dr. Ziobro is rated as an Experienced provider by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. She is also highly rated in 15 other conditions, according to our data. Her clinical expertise encompasses Seizures, Generalized Tonic-Clonic Seizure, Myoclonic Epilepsy, and Dravet Syndrome. Dr. Ziobro is board certified in Neurology W/Spec Qual Child Neuro and Epilepsy.
C. S. Mott Children's Hospital
Jessica Rieckhoff is a Nurse Practitioner practicing medicine in Ann Arbor, Michigan. Ms. Rieckhoff is rated as an Experienced provider by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. Her clinical expertise encompasses PEPCK 1 Deficiency, Autosomal Recessive Congenital Methemoglobinemia, Dihydrolipoamide Dehydrogenase Deficiency, and Pyruvate Carboxylase Deficiency. Ms. Rieckhoff is board certified in Acute Care Pediatric Nurse Pract.
C. S. Mott Children's Hospital
Martha Carlson is a Pediatrics specialist and a Pediatric Neurologist practicing medicine in Ann Arbor, Michigan. Dr. Carlson is rated as an Experienced provider by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. She is also highly rated in 41 other conditions, according to our data. Her clinical expertise encompasses Autism Spectrum Disorder, Seizures, Stereotypic Movement Disorder, and Spasmus Nutans.
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Sucheta Joshi is a Neurologist practicing medicine in Ann Arbor, Michigan. Dr. Joshi is rated as an Advanced provider by MediFind in the treatment of Dihydrolipoamide Dehydrogenase Deficiency. She is also highly rated in 29 other conditions, according to our data. Her clinical expertise encompasses West Syndrome, Epilepsy in Children, Epilepsy, and Seizures.
C. S. Mott Children's Hospital
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 Dihydrolipoamide Dehydrogenase 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.
Last Updated: 04/28/2026





