The 20 Best Maple Syrup Urine Disease Doctors Near Me in Chicago, IL

Carlos Prada is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chicago, Illinois. Dr. Prada is rated as a Distinguished provider by MediFind in the treatment of Maple Syrup Urine Disease. He is also highly rated in 171 other conditions, according to our data. His clinical expertise encompasses RASopathies, Smith-Kingsmore Syndrome, Neurofibromatosis Type 1 (NF1), and Neurofibromatosis.

Joel Charrow is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chicago, Illinois. Dr. Charrow is rated as a Distinguished provider by MediFind in the treatment of Maple Syrup Urine Disease. He is also highly rated in 45 other conditions, according to our data. His clinical expertise encompasses Gaucher Disease Type 1, Gaucher Disease, Achondroplasia, Isovaleric Acidemia, and Splenectomy.

Joshua Baker is a Pediatrics provider practicing medicine in Chicago, Illinois. Dr. Baker is rated as an Advanced provider by MediFind in the treatment of Maple Syrup Urine Disease. He is also highly rated in 152 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Acid Sphingomyelinase Deficiency (ASMD), and Propionic Acidemia.

George Hoganson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chicago, Illinois. Dr. Hoganson is rated as an Experienced provider by MediFind in the treatment of Maple Syrup Urine Disease. He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Isovaleric Acidemia, Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.

Mickey Kuo is a Medical Genetics provider practicing medicine in Maywood, Illinois. Dr. Kuo is rated as an Experienced provider by MediFind in the treatment of Maple Syrup Urine Disease. His clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Inborn Amino Acid Metabolism Disorder, Fabry Disease, and CHST3-Related Skeletal Dysplasia.