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HYPEROXALURIA IN CHILDREN

By Manel Jellouli

HYPEROXALURIA IN CHILDREN Law

HYPEROXALURIA IN CHILDREN

0 - Default Title
Description
Primary hyperoxaluria is a group of inherited diseases with autosomal recessive inheritance (ARD), resulting from an inborn disorder of hepatic glyoxylate metabolism responsible for excessive oxalate production and increased urinary oxalate excretion.This disorder leads to precipitation of highly insoluble oxalate in the form of calcium oxalate crystals in the kidneys, resulting in nephrocalcinosis, recurrent urinary lithiasis (LU) and frequent progression to chronic renal failure (CKD). When renal function is impaired, elevated oxalemia leads to systemic oxalosis, corresponding to calcium oxalate deposition in various tissues, mainly bone, but also the cardiovascular system, skin, retina, etc.
Product details
Binding:
Paperback
Number of Pages:
52
Release Date:
2023-11-24
Publication Date:
2023-11-24
Publisher:
Our Knowledge Publishing
Languages:
Original: English
ISBN10:
6206600947
ISBN13:
9786206600947
GPSR Manufacturer Reference:
[email protected]
Weight:
96 g
Height:
150 cm
Width:
220 cm
Thickness:
4 cm
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