clinical and para clinical findings in the children with tyrosinemia referring for liver transplantation
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Clinical and Para Clinical Findings in the Children with Tyrosinemia Referring for Liver Transplantation
BACKGROUND Hereditary tyrosinemia type 1 (HT1) is a rare autosomal recessive inborn error of metabolism caused by deficiency of fumarylacetoacetate hydrolase enzyme. This disease manifests with severe liver and kidney impairment and is associated with an increased risk of liver cancer. The aim of this study was to evaluate clinical, laboratory, imaging, and histopathologic characteristics in th...
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Background: Despite close monitoring of transplant patients, cytomegalovirus (CMV) infection remains one of the most critical problems in the field of transplantation. This study aims to investigate the relationship between CMV viral load and clinical laboratory findings in transplant recipients. Materials And Methods: Thirty-four transplant recipients comprising 15 kidney transplant (KT) reci...
متن کاملResolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatoma.
The clinical history before transplantation and subsequent clinical and biochemical course of 3 children and one adult with hereditary tyrosinemia treated by orthotopic hepatic transplantation is described. All four patients are now free of their previous dietary restrictions and appear to be cured of both their metabolic disease and their hepatic neoplasm.
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عنوان ژورنال:
international journal of preventive medicineجلد ۴، شماره ۱۲، صفحات ۱۳۸۰-۰
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