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Tyrosinemia type 2

Richner-Hanhart syndromeOculocutaneous 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
Long Term Safety Study of Orfadin Treatment in HT-1 Patients in Standard Clinical Care
Status: Recruiting
Last Changed: Mar 05, 2019
First Received: Dec 19, 2014
Disease(s): Hereditary Tyrosinemia, Type I
Intervention(s): Nitisinone
Locations: Swedish Orphan Biovitrum Investigational Site, Innsbruck, Austria
Swedish Orphan Biovitrum Investigational Site, Wien, Austria
Swedish Orphan Biovitrum Investigational Site, Antwerpen, Belgium
Swedish Orphan Biovitrum Investigational Site, Brussels, Belgium
Swedish Orphan Biovitrum Investigational Site, Leuven, Belgium
... and 70 other locations.
Biomarker for the Early Diagnosis and Monitoring in Tyrosinemia Type 1 (BioTyrosin)
Status: Recruiting
Last Changed: May 15, 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