The 20 Best Galactosemia Doctors in The United States
Find the Top Galactosemia Experts and Specialists
St. Christopher's Pediatric Associates Genetics - E. Erie Avenue
Anthony Perszyk is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Perszyk is rated as an Experienced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 11 other conditions, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Mucolipidosis 3. Dr. Perszyk is board certified in American Board Of Medical Genetics And Genomics. Dr. Perszyk is currently accepting new patients.
State University Of Iowa
Amy Calhoun is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Iowa City, Iowa. Dr. Calhoun is rated as an Experienced provider by MediFind in the treatment of Galactosemia. She is also highly rated in 9 other conditions, according to our data. Her clinical expertise encompasses Wolf-Hirschhorn Syndrome, Otospondylomegaepiphyseal Dysplasia, MELAS Syndrome, Costello Syndrome, and Spinal Fusion. Dr. Calhoun is currently accepting new patients.
Childrens Health Care Associates Inc
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Ficicioglu is rated as a Distinguished provider by MediFind in the treatment of Galactosemia. He is also highly rated in 51 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Urea Cycle Disorders (UCD), and Gaucher Disease.
Duke University Hospital
Dwight Koeberl is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Durham, North Carolina. Dr. Koeberl is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 16 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Von Gierke Disease, Propionic Acidemia, and X-Linked Creatine Deficiency. Dr. Koeberl is board certified in American Board Of Medical Genetics, Clinical Biochemical Genetics , American Board Of Medical Genetics, Clinical Genetics And Genomics - General , and American Board Of Pediatrics, General Pediatrics. Dr. Koeberl is currently accepting new patients.
University Of Michigan Pediatric Genetics Clinic
Amanda Pritchard is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Pritchard is rated as an Advanced provider by MediFind in the treatment of Galactosemia. She is also highly rated in 150 other conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and 47 XYY Syndrome. Dr. Pritchard is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2019 , American Board Of Pediatrics, Pediatrics - 2016, and American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2019 . Dr. Pritchard is currently accepting new patients.
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 Galactosemia. She is also highly rated in 45 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Danon Disease, Von Gierke Disease, and Tyrosinemia Type 1. Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Ahmad is currently accepting new patients.
Corewell Health Grand Rapids Hospitals Biochemical Genetics - 25 Michigan St NE
Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Galactosemia. 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 and American Board Of Pediatrics. Dr. Priestley is currently accepting new patients.
Pediatric Otolaryngology Clinic
Kristen Lee is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Galactosemia. She is also highly rated in 139 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, Medical Biochemical Genetics, and Clinical Genetics & Genomics. Dr. Lee is currently accepting new patients.
Emory Clinic At 1365 Clifton Road
William Wilcox is a Medical Genetics provider practicing medicine in Atlanta, Georgia. Dr. Wilcox is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 25 other conditions, according to our data. His clinical expertise encompasses Fabry Disease, Achondroplasia, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). Dr. Wilcox is board certified in American Board Of Medical Genetics And Genomics, 1996. Dr. Wilcox is currently accepting new patients.
University Of Michigan Pediatric Genetics Clinic
Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Quinonez is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 130 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Propionic Acidemia. Dr. Quinonez is board certified in Pediatrics, American Board Of Pediatrics, Pediatrics - 2011, Clinical Biochemical Genetics, American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2015 , American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2024 , and Clinical Genetics & Genomics. Dr. Quinonez is currently accepting new patients.
UT Southwestern - Pediatrics
Luis Umana is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 178 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Dr. Umana is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Olaf Bodamer is a Medical Genetics provider practicing medicine in Boston, Massachusetts. Dr. Bodamer is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 51 other conditions, according to our data. His clinical expertise encompasses Kabuki Syndrome, Classic Galactosemia, Niemann-Pick Disease, and Mucopolysaccharidoses (MPS). Dr. Bodamer is currently accepting new patients.
Walla Al-Hertani is a Medical Genetics provider practicing medicine in Orange, California. Dr. Al-Hertani is rated as an Advanced provider by MediFind in the treatment of Galactosemia. She is also highly rated in 62 other conditions, according to our data. Her clinical expertise encompasses Von Gierke Disease, Classic Galactosemia, Phosphoglycerate Kinase Deficiency, and Glycogen Storage Disease Type 13. Dr. Al-Hertani is currently accepting new patients.
Lpch Medical Group Div Of Lucile
Gregory Enns is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Enns is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 56 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Arginase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Enns is currently accepting new patients.
Jared Hamm is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Knoxville, Tennessee. Dr. Hamm is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 182 other conditions, according to our data. His clinical expertise encompasses Clouston Syndrome, AEC Syndrome, Zlotogora-Ogur Syndrome, and EEC Syndrome. Dr. Hamm is currently accepting new patients.
Richard Chang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chang is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 156 other conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Maternal Hyperphenylalaninemia, and Adrenoleukodystrophy (ALD). Dr. Chang is currently accepting new patients.
Icahn School Of Medicine At Mount Sinai
Mary Lopiccolo is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Lopiccolo is rated as an Advanced provider by MediFind in the treatment of Galactosemia. She is also highly rated in 30 other conditions, according to our data. Her clinical expertise encompasses Glutaric Acidemia Type 2, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Carnitine Palmitoyltransferase 2 Deficiency.
Mainehealth
Wendy Smith is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Portland, Maine. Dr. Smith is rated as an Advanced provider by MediFind in the treatment of Galactosemia. She is also highly rated in 14 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and MELAS Syndrome.
Iu Health Medical Group Riley Specialists LLC
Molly Mcpheron is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Indianapolis, Indiana. Dr. Mcpheron is rated as an Advanced provider by MediFind in the treatment of Galactosemia. She is also highly rated in 136 other conditions, according to our data. Her clinical expertise encompasses Ornithine Transcarbamylase Deficiency, Pompe Disease, Phenylketonuria (PKU), and Danon Disease. Dr. Mcpheron is currently accepting new patients.
Kaiser Permanente Los Angeles Medical Center - Genetics Department
Divya Vats is a Medical Genetics provider practicing medicine in Los Angeles, California. Dr. Vats is rated as an Advanced provider by MediFind in the treatment of Galactosemia. He is also highly rated in 25 other conditions, according to our data. His clinical expertise encompasses Adrenoleukodystrophy (ALD), Thymidine Kinase 2 Deficiency (TK2d), Classic Galactosemia, and Dihydropteridine Reductase Deficiency. Dr. Vats is currently accepting new patients.
Last Updated: 11/08/2026






