MediFind found 403 doctor with experience in Tyrosinemia Type 1. Of these, 294 are Experienced, 97 are Advanced, 10 are Distinguished and 2 are Elite.
Willem Van Ginkel practices in Groningen, Netherlands. Van Ginkel is rated as an Elite expert by MediFind in the treatment of Tyrosinemia Type 1. Their top areas of expertise are Tyrosinemia Type 1, Phenylketonuria (PKU), Porphyria, and Vitamin B12 Deficiency Anemia.
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Markus Grompe is a Pediatrics specialist and a Medical Genetics provider in Portland, Oregon. Dr. Grompe is rated as an Elite provider by MediFind in the treatment of Tyrosinemia Type 1. His top areas of expertise are Congenital Aplastic Anemia, Tyrosinemia Type 1, Phenylketonuria (PKU), Islet Cell Transplantation, and Hepatectomy.
Margaretha Fokkema-Heiner practices in Groningen, Netherlands. Ms. Fokkema-Heiner is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Tyrosinemia Type 1, Phenylketonuria (PKU), Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Kidney Transplant, and Ileostomy.
Kimber Van Vliet practices in Groningen, Netherlands. Ms. Van Vliet is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Tyrosinemia Type 1, Phenylketonuria (PKU), and Vitamin B12 Deficiency Anemia.
Francjan Van Spronsen practices in Groningen, Netherlands. Van Spronsen is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Their top areas of expertise are Phenylketonuria (PKU), Tyrosinemia Type 1, Maternal Hyperphenylalaninemia, and Molybdenum Cofactor Deficiency (MoCD).
Francjan Van Spronsen-Spronsen practices in Groningen, Netherlands. Van Spronsen-Spronsen is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Their top areas of expertise are Phenylketonuria (PKU), Tyrosinemia Type 1, Maternal Hyperphenylalaninemia, and Molybdenum Cofactor Deficiency (MoCD).
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Peter Baker is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Baker is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 1. His top areas of expertise are Tyrosinemia Type 2, Tyrosinemia Type 3, Tyrosinemia Type 1, and Maple Syrup Urine Disease. Dr. Baker is currently accepting new patients.
Anita Macdonald practices in Birmingham, United Kingdom. Ms. Macdonald is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Tyrosinemia Type 1, Gastrostomy, and Liver Embolization.
Philippe Goyens practices in Brussels, Belgium. Mr. Goyens is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. His top areas of expertise are Tyrosinemia Type 1, Hirschsprung Disease, Phenylketonuria (PKU), and Malnutrition.
Carolina Arias practices in Santiago, Chile. Ms. Arias is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Tyrosinemia Type 1, Phenylketonuria (PKU), Maple Syrup Urine Disease, and Dihydrolipoamide Dehydrogenase Deficiency.
Marelle Bouva practices in Bilthoven, Netherlands. Ms. Bouva is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Tyrosinemia Type 1, Classic Galactosemia, Neonatal Hypothyroidism, and Adrenoleukodystrophy (ALD).
Veronica Cornejo practices in Santiago, Chile. Ms. Cornejo is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Tyrosinemia Type 1, Phenylketonuria (PKU), Dihydrolipoamide Dehydrogenase Deficiency, and Maple Syrup Urine Disease.
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Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as an Experienced provider by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation.
Richard Chang is a Medical Genetics provider in Orange, California. Dr. Chang is rated as an Experienced provider by MediFind in the treatment of Tyrosinemia Type 1. His top areas of expertise are Citrullinemia, Beta-Ketothiolase Deficiency, Urea Cycle Disorders (UCD), and Biotinidase Deficiency. Dr. Chang is currently accepting new patients.
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Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Breilyn is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 1. Her top areas of expertise are Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Tyrosinemia Type 3.
Genevieve Morrow practices in Quebec, Canada. Ms. Morrow is rated as an Advanced expert by MediFind in the treatment of Tyrosinemia Type 1. Her top area of expertise is Tyrosinemia Type 1.
Luis Umana is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 1. His top areas of expertise are Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Classic Galactosemia, Biotinidase Deficiency, and Argininosuccinic Aciduria.
Robert Tanguay practices in Quebec, Canada. Mr. Tanguay is rated as an Advanced expert by MediFind in the treatment of Tyrosinemia Type 1. His top area of expertise is Tyrosinemia Type 1.
Jan Haavik practices in Bergen, Norway. Haavik is rated as an Advanced expert by MediFind in the treatment of Tyrosinemia Type 1. Their top areas of expertise are Attention Deficit Hyperactivity Disorder (ADHD), Tyrosinemia Type 1, Autism Spectrum Disorder, and Bipolar Disorder (BPD).
Stephan Huijbregts practices in Leiden, Netherlands. Mr. Huijbregts is rated as an Advanced expert by MediFind in the treatment of Tyrosinemia Type 1. His top areas of expertise are Phenylketonuria (PKU), Tyrosinemia Type 1, Neurofibromatosis Type 1 (NF1), and Neurofibromatosis.
Last Updated: 01/09/2026