MediFind found 5 doctor with experience in Galactose Epimerase Deficiency near Indiana, US. Of these, 3 are Advanced and 2 are Experienced.
University Family Physicians, Inc.
Molly Mcpheron is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Mcpheron is rated as an Advanced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Pompe Disease, Danon Disease, Phenylketonuria (PKU), and Maternal Hyperphenylalaninemia. Dr. Mcpheron is currently accepting new patients.
University Family Physicians, Inc.
Bryan Hainline is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Hainline is rated as an Advanced provider by MediFind in the treatment of Galactose Epimerase Deficiency. His top areas of expertise are Phenylketonuria (PKU), Pyruvate Carboxylase Deficiency, Urea Cycle Disorders (UCD), and Inborn Amino Acid Metabolism Disorder. Dr. Hainline is currently accepting new patients.
University Family Physicians, Inc.
Melissa Lah is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Lah is rated as an Advanced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Prader-Willi Syndrome, Maternal Hyperphenylalaninemia, and Miller-Dieker Syndrome. Dr. Lah is currently accepting new patients.
Brett Graham is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Graham is rated as an Experienced provider by MediFind in the treatment of Galactose Epimerase Deficiency. His top areas of expertise are MELAS Syndrome, Mitochondrial Complex 1 Deficiency, Smith-Magenis Syndrome, and Hypotonia. Dr. Graham is currently accepting new patients.
University Family Physicians, Inc.
Erin Conboy is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Conboy is rated as an Experienced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Hereditary Multiple Osteochondromas, Ectodermal Dysplasias, Clouston Syndrome, and Early Infantile Epileptic Encephalopathy. Dr. Conboy is currently accepting new patients.
Last Updated: 10/30/2025