The 20 Best Galactose Epimerase Deficiency Doctors in The United States

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 Galactose Epimerase Deficiency. He is also highly rated in 11 other conditions, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Mucolipidosis 3. Dr. Perszyk is board certified in American Board Of Medical Genetics And Genomics. Dr. Perszyk is currently accepting new patients.

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 Galactose Epimerase Deficiency. She is also highly rated in 9 other conditions, according to our data. Her clinical expertise encompasses Wolf-Hirschhorn Syndrome, Otospondylomegaepiphyseal Dysplasia, MELAS Syndrome, and Costello Syndrome. Dr. Calhoun is currently accepting new patients.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. 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 Costello 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.

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 Galactose Epimerase Deficiency. 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 3. Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Ahmad is currently accepting new patients.

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 Galactose Epimerase Deficiency. She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase 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.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. 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 Maple Syrup Urine Disease. 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.

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 Galactose Epimerase Deficiency. 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 Argininosuccinic Aciduria. Dr. Umana is currently accepting new patients.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. He is also highly rated in 54 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.

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 Galactose Epimerase Deficiency. She is also highly rated in 62 other conditions, according to our data. Her clinical expertise encompasses Von Gierke Disease, Classic Galactosemia, Andersen Disease, and Glycogen Storage Disease Type 0. Dr. Al-Hertani 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 Galactose Epimerase Deficiency. He is also highly rated in 182 other conditions, according to our data. His clinical expertise encompasses AEC Syndrome, EEC Syndrome, Zlotogora-Ogur Syndrome, and Clouston Syndrome. Dr. Hamm is currently accepting new patients.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. 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.

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 Galactose Epimerase Deficiency. She is also highly rated in 15 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and MELAS Syndrome.

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 Galactose Epimerase Deficiency. 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 Maternal Hyperphenylalaninemia. Dr. Vats is currently accepting new patients.