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1. 小児における慢性腎臓病の疫学、病因、および経過 epidemiology etiology and course of chronic kidney disease in children
2. 慢性腎疾患関連眼疾患 eye disorders associated with chronic kidney disease
3. 原発性高シュウ酸尿症 primary hyperoxaluria
4. 腎臓の同種移植片機能不全の鑑別診断 differential diagnosis of renal allograft dysfunction
5. 腎石灰沈着症 nephrocalcinosis

English Journal

Reduction of plasma oxalate levels by oral application of Oxalobacter formigenes in 2 patients with infantile oxalosis.

Hoppe B, Dittlich K, Fehrenbach H, Plum G, Beck BB.SourceDepartment of Pediatric and Adolescent Medicine, Division of Pediatric Nephrology, University Hospital, Cologne, Germany. bernd.hoppe@uk-koeln.de
American journal of kidney diseases : the official journal of the National Kidney Foundation.Am J Kidney Dis.2011 Sep;58(3):453-5. Epub 2011 Jun 25.
The spectrum of primary hyperoxaluria type I is extremely heterogeneous, ranging from singular to recurrent urolithiasis and early end-stage renal disease (ESRD). In infantile oxalosis, the most devastating form, ESRD occurs as early as within the first weeks of life. No kidney replacement therapy s
PMID 21705122

Combined split liver and kidney transplantation in a three-year-old child with primary hyperoxaluria type 1 and complete thrombosis of the inferior vena cava.

Khan Z, Sciveres M, Salis P, Minervini M, Maggiore G, Cintorino D, Riva S, Gridelli B, Emma F, Spada M.SourceUniversity of Pittsburgh School of Medicine, Medical Scientist Training Program, Pittsburgh, PA, USA.
Pediatric transplantation.Pediatr Transplant.2011 Jun;15(4):E64-70. doi: 10.1111/j.1399-3046.2009.01241.x. Epub 2009 Sep 28.
PH1 is an inborn error of the metabolism in which a functional deficiency of the liver-specific peroxisomal enzyme, AGT, causes hyperoxaluria and hyperglycolic aciduria. Infantile PH1 is the most aggressive form of this disease, leading to early nephrocalcinosis, systemic oxalosis, and end-stage ren
PMID 19793227