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Verfasst von:Morath, Marina [VerfasserIn]   i
 Hörster, Friederike [VerfasserIn]   i
 Sauer, Sven [VerfasserIn]   i
Titel:Renal dysfunction in methylmalonic acidurias
Titelzusatz:review for the pediatric nephrologist
Verf.angabe:Marina A. Morath, Friederike Hörster, Sven W. Sauer
Jahr des Originals:2012
Umfang:9 S.
Fussnoten:First Online: 20 July 2012 ; Gesehen am 07.05.2018
Titel Quelle:Enthalten in: Pediatric nephrology
Jahr Quelle:2013
Band/Heft Quelle:28(2013), 2, S. 227-235
ISSN Quelle:1432-198X
Abstract:Methylmalonic acidurias are a heterogeneous group of inborn errors of branched-chain amino acid metabolism. Depending on the underlying etiology, acute or chronic renal disease constitutes major (long-term) complications. In recent decades, overall survival has improved due to optimized treatment strategies based on the use of standardized emergency protocols and dialysis techniques. The majority of these patients, especially those having mut°, cblB, and cblA deficiency, are at increased risk of developing chronic kidney disease secondary to tubulointerstitial nephritis to require hemo- or peritoneal dialysis. Kidney and/or liver transplantation, as organ replacement, or even gene therapy on a limited scale, are controversially discussed treatment options in methylmalonic acidurias. The pathophysiological basis of renal disease has not been clarified in detail until now, but a severe mitochondrial dysfunction and an impairment of tubular dicarboxylic acid transport due to accumulated toxic metabolic compounds has been recently proposed. Another severe renal complication of methylmalonic acidurias is the occurrence of cblC-associated infantile atypical hemolytic syndrome, which can result in acute kidney injury. Close collaboration between (pediatric) nephrologists and metabolic specialists is required for the long-term management of these patients.
DOI:doi:10.1007/s00467-012-2245-2
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Verlag: http://dx.doi.org/10.1007/s00467-012-2245-2
 Verlag: https://link.springer.com/article/10.1007/s00467-012-2245-2
 DOI: https://doi.org/10.1007/s00467-012-2245-2
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1573995126
Verknüpfungen:→ Zeitschrift

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