CareLit · DOI-Nachweis · Klinische Pädiatrie
Primary Hyperoxaluria Type 1: A Cause for Infantile Renal Failure and Massive Nephrocalcinosis
DOI 10.1055/s-0035-1554638
Bibliografische Angaben
Nachweis in CareLit
Autor:innenN.N.
ZeitschriftKlinische Pädiatrie
Ausgabe05/2015
Jahrgang / SeitenJg. 227 · S. 293-295
Kernaussage aus der Literatur
Abstract-Vorschau
Abstract Primary hyperoxaluria type 1 is a rare autosomal-recessive disease caused by the deficient activity of the liver specific enzyme alanine-glyoxylate aminotransferase. Increased endogenous oxalate production induces severe hyperoxaluria, recurrent urolithiasis, progressive nephrocalcinosis and renal failure. Here we report a 6 month old boy who presented with vomiting and decreased urine volume. He was diagno…
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Zitierempfehlung
N.N (2015) Primary Hyperoxaluria Type 1: A Cause for Infantile Renal Failure and Massive Nephrocalcinosis. Klinische Pädiatrie, 227 (05), 293-295. https://doi.org/10.1055/s-0035-1554638
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