Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1

Primary hyperoxaluria type 1 results from alanine:glyoxylate aminotransferase deficiency. Due to genotype/phenotype heterogeneity in this autosomal recessive disorder, the renal outcome is difficult to predict in these patients and the long-term impact of conservative management in children is unkno...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Kidney international 2009-10, Vol.76 (7), p.767-773
Hauptverfasser:	Fargue, Sonia, Harambat, Jérôme, Gagnadoux, Marie-France, Tsimaratos, Michel, Janssen, Françoise, Llanas, Brigitte, Berthélémé, Jean-Pierre, Boudailliez, Bernard, Champion, Gérard, Guyot, Claude, Macher, Marie-Alice, Nivet, Hubert, Ranchin, Bruno, Salomon, Rémi, Taque, Sophie, Rolland, Marie-Odile, Cochat, Pierre
Format:	Artikel
Sprache:	eng
Schlagworte:	Age of Onset Biological and medical sciences Child Child, Preschool Disease Management Errors of metabolism Glomerular Filtration Rate Humans Hyperoxaluria, Primary - complications Hyperoxaluria, Primary - diagnosis Hyperoxaluria, Primary - therapy Kidney Diseases - etiology Kidney Diseases - physiopathology Kidney Diseases - prevention & control Medical sciences Metabolic diseases Miscellaneous hereditary metabolic disorders Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure orphan disease primary hyperoxaluria type 1 Renal failure renal insufficiency Retrospective Studies survival
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!