The 20 Best Tyrosinemia Type 3 Doctors in The United States

Tarachandra Narumanchi is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Narumanchi is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Narumanchi is board certified in American Board Of Medical Genetics And Genomics. Dr. Narumanchi is currently accepting new patients.

Peter Baker is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Aurora, Colorado. Dr. Baker is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 3. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Tyrosinemia Type 3, Tyrosinemia Type 2, Tyrosinemia Type 1, and Maple Syrup Urine Disease. Dr. Baker 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 Tyrosinemia Type 3. 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.

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 Tyrosinemia Type 3. 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.

Tomoyasu Higashimoto is a Medical Genetics provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. He is also highly rated in 110 other conditions, according to our data. His clinical expertise encompasses Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia. Dr. Higashimoto is board certified in Family Medicine and Clinical Genetics & Genomics. Dr. Higashimoto is currently accepting new patients.

Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Breilyn is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. She is also highly rated in 42 other conditions, according to our data. Her clinical expertise encompasses Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Phenylketonuria (PKU).

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 Tyrosinemia Type 3. 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.

Michele Spencer-Manzon is a Medical Genetics provider practicing medicine in New Haven, Connecticut. Dr. Spencer-Manzon is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. She is also highly rated in 14 other conditions, according to our data. Her clinical expertise encompasses Maple Syrup Urine Disease, Tyrosinemia Type 2, Tyrosinemia Type 3, and Tyrosinemia Type 1. Dr. Spencer-Manzon is currently accepting new patients.

Chung Lee is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. She has been practicing medicine for over 18 years. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. She is also highly rated in 45 other conditions, according to our data. Her clinical expertise encompasses Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, Maple Syrup Urine Disease, and Carnitine Palmitoyltransferase 2 Deficiency.

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 Tyrosinemia Type 3. 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.

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 Tyrosinemia Type 3. 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.

George Diaz is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Diaz is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Urea Cycle Disorders (UCD), and Ornithine Transcarbamylase Deficiency.

Laura Mackay is a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Mackay is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. She is also highly rated in 131 other conditions, according to our data. Her clinical expertise encompasses Isovaleric Acidemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Adrenoleukodystrophy (ALD). Dr. Mackay is currently accepting new patients.

Bryan Hainline is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Indianapolis, Indiana. Dr. Hainline is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. He is also highly rated in 69 other conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Pyruvate Carboxylase Deficiency, Urea Cycle Disorders (UCD), and Inborn Amino Acid Metabolism Disorder. Dr. Hainline is currently accepting new patients.

Christina Sloan-Heggen is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Sloan-Heggen is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. 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-Heggen is board certified in Medical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Sloan-Heggen is currently accepting new patients.

Cheryl Garganta is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Garganta is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Hyperlysinemia, Glutaric Acidemia Type 1, Tyrosinemia Type 3, and Tyrosinemia Type 1. Dr. Garganta is currently accepting new patients.

Laura Konczal is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Cleveland, Ohio. Dr. Konczal is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. She is also highly rated in 25 other conditions, according to our data. Her clinical expertise encompasses Gaucher Disease Type 3, Gaucher Disease Type 2, Gaucher Disease Type 1, and Gaucher Disease. Dr. Konczal is currently accepting new patients.

Janet Thomas is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Aurora, Colorado. Dr. Thomas is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Homocystinuria, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Thomas is currently accepting new patients.

Peter Leahy is a Medical Genetics specialist and an Oncologist practicing medicine in Oklahoma City, Oklahoma. Dr. Leahy is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. He is also highly rated in 147 other conditions, according to our data. His clinical expertise encompasses Thymidine Kinase 2 Deficiency (TK2d), Maple Syrup Urine Disease, Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.

Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Ficicioglu is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 3. 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.