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Type 1 Tyrosinemia with Hypophosphatemic Rickets; a Case Report
Type 1 Tyrosinemia with Hypophosphatemic Rickets; a Case Report

Peyman Eshraghi; Foad Faroughi; Mohammad Karim Alizadeh

Volume 2, Issue 3.3 , September 2014, , Pages 63-66

https://doi.org/10.22038/ijp.2014.2999

Abstract
  Background: Tyrosinemia type 1 is an autosomal recessive metabolic disorder, which typically affects liver and kidneys. It is caused by a defect in fumarylacetoacetate hydrolase or ...  Read More