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Coexistence of autosomal dominant polycystic kidney disease and neurofibromatosis: Report of a family

  • Meng Hao Chen
  • , Kuo Su Chen*
  • , Jia Woei Hou
  • , Ching Chang Lee
  • , Jen Seng Huang
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital

Research output: Contribution to journal › Journal Article › peer-review

7 Scopus citations

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) and neurofibromatosis are both autosomal dominant heredofamilial disorders. Concurrence of these two diseases is very rare. Herein, we report the coexistence of neurofibromatosis in 3 members, a mother and her 2 sons, of a family with preexisting ADPKD. The chromosomal studies of these patients show no translocation, deletion, or other gross abnormality. It is possible that a mutated neurofibromatosis gene developed in the ADPKD mother with subsequent inherence of both ADPKD and NF genes in her 2 sons.

Original languageEnglish
Pages (from-to)376-380
Number of pages5
JournalAmerican Journal of Nephrology
Volume22
Issue number4
DOIs
StatePublished - 2002
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Heredofamilial disorders
  • Neurofibromatosis
  • Polycystic kidney disease

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