Topics
morbidityDisease
autosomal recessiveDisease
kidney transplantationDisease
Primary hyperoxaluriaDisease
end-stage renal diseaseDisease
oxalateChemical substance
liverAnatomical structure
renal failureDisease
hemodialysisElection
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a deficiency of the hepatic enzyme alanine-glyoxylate aminotransferase leads to endogenous oxalate overproduction, renal failure, systemic oxalate deposition and death. As hemodialysis provides insufficient oxalate clearance, patients ultimately require both liver and kidney transplantation for correction of the metabolic abnormality and oxalate excretion. Herein, we describe a young adult male with end-stage renal disease and systemic oxalosis causing progressive disabling multi-organ dysfunction while awaiting transplantation. We review the literature regarding liver-kidney transplantation and suggest that for patients with PH1, a standardized ass...
Introduction. Primary hyperoxaluria type-1 (PHI) is an autosomal recessive disorder caused by impair...
Background: Kidney transplantation alone in Primary Hyperoxaluria is associated with a high rate of ...
Primary hyperoxaluria type 1 (PH1) usually presents with recurrent urolithiasis, nephrocalcinosis an...
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a defic...
Primary hyperoxaluria type I (PH1) is a rare hereditary metabolic disorder, due to the deficiency of...
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by the functional defect...
Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder in which deficiency of the...
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepat...
Primary hyperoxalurias (PH) are inborn errors in the metabolism of glyoxylate and oxalate. PH type 1...
BACKGROUND: Primary hyperoxaluria leads to oxalosis, a systemic illness with fatal prognosis in urem...
Primary hyperoxaluria type 1 (PH1) is a rare genetic disorder characterized by allelic and clinical ...
BACKGROUND: Primary hyperoxaluria leads to oxalosis, a systemic illness with fatal prognosis in urem...
Primary hyperoxaluria Type 1 is a rare autosomal recessive inborn error of glyoxylate metabolism, ca...
PH1 is a metabolic disorder characterized by urolithiasis and the accumulation of oxalate crystals i...
Primary hyperoxaluria type 1 (PH1) is a rare liver enzymatic defect that causes overproduction of pl...
Introduction. Primary hyperoxaluria type-1 (PHI) is an autosomal recessive disorder caused by impair...
Background: Kidney transplantation alone in Primary Hyperoxaluria is associated with a high rate of ...
Primary hyperoxaluria type 1 (PH1) usually presents with recurrent urolithiasis, nephrocalcinosis an...
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a defic...
Primary hyperoxaluria type I (PH1) is a rare hereditary metabolic disorder, due to the deficiency of...
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by the functional defect...
Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder in which deficiency of the...
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepat...
Primary hyperoxalurias (PH) are inborn errors in the metabolism of glyoxylate and oxalate. PH type 1...
BACKGROUND: Primary hyperoxaluria leads to oxalosis, a systemic illness with fatal prognosis in urem...
Primary hyperoxaluria type 1 (PH1) is a rare genetic disorder characterized by allelic and clinical ...
BACKGROUND: Primary hyperoxaluria leads to oxalosis, a systemic illness with fatal prognosis in urem...
Primary hyperoxaluria Type 1 is a rare autosomal recessive inborn error of glyoxylate metabolism, ca...
PH1 is a metabolic disorder characterized by urolithiasis and the accumulation of oxalate crystals i...
Primary hyperoxaluria type 1 (PH1) is a rare liver enzymatic defect that causes overproduction of pl...
Introduction. Primary hyperoxaluria type-1 (PHI) is an autosomal recessive disorder caused by impair...
Background: Kidney transplantation alone in Primary Hyperoxaluria is associated with a high rate of ...
Primary hyperoxaluria type 1 (PH1) usually presents with recurrent urolithiasis, nephrocalcinosis an...
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