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

Research output: Contribution to journalJournal 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

Keywords

  • Heredofamilial disorders
  • Neurofibromatosis
  • Polycystic kidney disease

Fingerprint

Dive into the research topics of 'Coexistence of autosomal dominant polycystic kidney disease and neurofibromatosis: Report of a family'. Together they form a unique fingerprint.

Cite this