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Primary hyperoxaluria

Primary hyperoxaluria is a rare condition (autosomal recessive), resulting in increased excretion of oxalate (up to 600mg a day from normal 50mg a day), with oxalate stones being common. Primary hyperoxaluria is a rare condition (autosomal recessive), resulting in increased excretion of oxalate (up to 600mg a day from normal 50mg a day), with oxalate stones being common. The buildup of oxalate in the body causes increased renal excretion of oxalate (hyperoxaluria), which in turn results in renal and bladder stones. Stones cause urinary obstruction (often with severe and acute pain), secondary infection of urine and eventually kidney damage.

[ "Disease", "Kidney", "Enzyme", "Oxalate", "Transplantation", "HOGA1 gene", "GRHPR gene", "Primary Hyperoxaluria Type I", "Primary Hyperoxaluria Type III", "Secondary hyperoxaluria" ]
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