Hyperoxaluries massives [Massive hyperoxaluria]

Details

Serval ID
serval:BIB_B8BA1F261657
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Hyperoxaluries massives [Massive hyperoxaluria]
Journal
Revue médicale de la Suisse romande
Author(s)
Barbey F., Cachat F., Nguyen Q.V., Rotman S., Burnier M., Daudon M.
ISSN
0035-3655
Publication state
Published
Issued date
2004
Volume
124
Number
8
Pages
477-82
Language
french
Notes
Publication types: Case Reports ; English Abstract ; Journal Article ; Review - Publication Status: ppublish
Abstract
Primary hyperoxaluria type I is a rare inborn error of metabolism caused by a deficiency of a liver-specific peroxisomal enzyme. It manifests by increased oxalate production that ultimately results in kidney failure, due to urolithiasis and nephrocalcinosis, and finally induces systemic oxalosis and risk of premature death. Primary hyperoxaluria type 2 is mainly responsible of urolithiasis. Enteric hyperoxaluria is a commonly seen adverse event of Crohn disease or after extensive intestinal resection. These affections represent the main etiologies of massive hyperoxaluria. If not recognized very soon and adequately treated, these conditions can progress rapidly to end stage renal failure.
Keywords
Child, Female, Humans, Hyperoxaluria, Primary, Male, Middle Aged
Pubmed
Create date
25/01/2008 12:55
Last modification date
20/08/2019 15:26
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