Renal transplantation in patients with Alport syndrome: patient selection, outcomes, and donor evaluation
- PMID: 30410383
- PMCID: PMC6198874
- DOI: 10.2147/IJNRD.S150539
Renal transplantation in patients with Alport syndrome: patient selection, outcomes, and donor evaluation
Abstract
Alport syndrome is an inherited disorder of basement membrane collagen IV that frequently results in end-stage renal disease. Patients with Alport syndrome who undergo renal transplantation have generally excellent outcomes. Posttransplant antiglomerular basement membrane nephritis is a rare complication of renal transplantation for Alport syndrome. Because Alport syndrome is a genetic disorder, potential related donors must be carefully evaluated in order to minimize harm.
Keywords: Alport syndrome; collagen IV; kidney transplantation; posttransplant anti-GBM nephritis.
Conflict of interest statement
Disclosure The author reports no conflicts of interest in this work.
References
- 
    - Kashtan CE, Ding J, Garosi G, et al. Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group. Kidney Int. 2018;93(5):1045–1051. - PubMed
 
- 
    - Fallerini C, Dosa L, Tita R, et al. Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases. Clin Genet. 2014;86(3):252–257. - PubMed
 
- 
    - Jais JP, Knebelmann B, Giatras I, et al. X-linked Alport syndrome: natural history in 195 families and genotype-phenotype correlations in males. J Am Soc Nephrol. 2000;11(4):649–657. - PubMed
 
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