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Tyrosinemia type 1

Fumarylacetoacetase deficiencyHypertyrosinemiaHepatorenal tyrosinemia
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-3 of 3 results.
Hereditary Hepatorenal Tyrosinemia Natural History in Egypt and the Arab World (Multicenter Clinical Study)
Status: Recruiting
Last Changed: Jan 10, 2019
First Received: Feb 27, 2018
Disease(s): Hereditary Tyrosinemia, Type I
Locations: Professor Yassin Abdel Ghaffar Charity Center for Liver Disease and Research, Nasr City, Cairo, Egypt
Biomarker for the Early Diagnosis and Monitoring in Tyrosinemia Type 1 (BioTyrosin)
Status: Recruiting
Last Changed: Sep 17, 2019
First Received: Sep 15, 2017
Disease(s): Tyrosinosis, Hepatorenal Tyrosinemia, Fumarylacetoacetase Deficiency, Fah Deficiency, Metabolic Disorders
Locations: Children Hospital, Faculty of Medicine, Cairo University, Cairo, Egypt
Centogene AG, Rostock, Germany
NIRMAN Navi Mumbai Institute of Research In Mental And Neurological Handicap/Pediatric Geneticist, Mumbai, India
Bio Equivalency 20 Mgm Orfadin and 20 Mgm of Nitisonine
Status: Not yet recruiting
Last Changed: Oct 03, 2019
First Received: Oct 03, 2019
Disease(s): Hereditary Tyrosinemia, Type I
Intervention(s): Nitisinone, Orfadin
Locations: Lifein Multi-Specialty Hospital, Navsari, Gujarat, India