Hyperoxaluria, primary, type I

*Gene map locus 2q36-q37

Alanine-glyoxylate aminotransferase deficiency

Glycolic aciduria

HP1

Hepatic AGT deficiency

Oxalosis I

Peroxisomal alanine:glyoxylate aminotransferase deficiency

Serine:pyruvate aminotransferase deficiency

[Clinical features: continuous, high urinary oxalate excretion; progressive bilateral oxalate urolithiasis and nephrocalcinosis]

[Inheritance: autosomal recessive]

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Primary Oxalosis With Cardiac Involvement : Echocardiographic Features of an Unusual Form of Cardiomyopathy	Primary Oxalosis With Cardiac Involvement : Echocardiographic Features of an Unusual Form of Cardiomyopathy	Persistent cutaneous manifestations of hyperoxaluria after combined hepatorenal transplantation
Circulation	Circulation	Dermatology Online Journal


Small intestinal infarction: a fatal complication of systemic oxalosis	The Primary Hyperoxalurias	A stony history
Journal of Clinical Pathology	Journal of the American Society of Nephrology	Nephrology Dialysis Transplantation


Late-onset primary hyperoxaluria diagnosed after renal transplantation presented with early recurrence of disease	Late-onset primary hyperoxaluria diagnosed after renal transplantation presented with early recurrence of disease	Oxalate deposition in tissues
Nephrology Dialysis Transplantation	Nephrology Dialysis Transplantation	Nephrology Dialysis Transplantation


Oxalate deposition in tissues	Oxalosis with nephrocalcinosis	Oxalosis with nephrocalcinosis
Nephrology Dialysis Transplantation	Nephrology Dialysis Transplantation	Nephrology Dialysis Transplantation


Oxalosis with nephrocalcinosis	Ulcerating subcutaneous nodules and advanced renal failure: is it time for a new liver?	Ulcerating subcutaneous nodules and advanced renal failure: is it time for a new liver?
Nephrology Dialysis Transplantation	Nephrology Dialysis Transplantation	Nephrology Dialysis Transplantation

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