Renal transplantation in patients with atypical haemolytic uraemic syndrome: a tailor made approach is necessary

van der Wijk, J., Smid, W. M., Seelen, M. A., de Kar, N. C. V., Offerman, J. J. G. & van Son, W. J., Jun-2011, In : Netherlands Journal of Medicine. 69, 6, p. 279-280 2 p.

Research output: Contribution to journalArticleAcademicpeer-review

  • J. van der Wijk
  • W. M. Smid
  • M. A. Seelen
  • N. C. van de Kar
  • J. J. G. Offerman
  • W. J. van Son

A 33-year-old woman with a history of chronic transplant dysfunction because of repeated bouts of haemolytic uraemic syndrome (HUS) was considered for a second transplant. Extensive genetic investigation of the complement system was executed to rule out known mutations prone to development of HUS. This case illustrates the importance of genetic screening in patients with recurrent HUS.

Original languageEnglish
Pages (from-to)279-280
Number of pages2
JournalNetherlands Journal of Medicine
Issue number6
Publication statusPublished - Jun-2011


  • Atypical haemolytic uremic syndrome, transplantation, factor H, COMPLEMENT-FACTOR-H, MUTATIONS, IMPACT, DISEASE, KIDNEY, AHUS

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