Coexistence of thin membrane and alport nephropathies in families with haematuria

Pediatr Nephrol. 1999 Nov;13(9):778-81. doi: 10.1007/s004670050699.

Abstract

The finding of familial haematuria without a history of deafness or renal impairment is often assumed to indicate a benign prognosis. However, we describe three families in whom Alport and thin basement membrane nephropathy were separately identified within the same pedigree. Our findings illustrate the importance of fully investigating families with haematuria, even if thin basement nephropathy has been diagnosed in one member.

Publication types

  • Case Reports

MeSH terms

  • Basement Membrane / pathology
  • Basement Membrane / ultrastructure
  • Child
  • Child, Preschool
  • Female
  • Hematuria / complications*
  • Hematuria / genetics
  • Humans
  • Kidney Diseases / complications*
  • Kidney Diseases / genetics
  • Kidney Diseases / pathology
  • Male
  • Microscopy, Electron
  • Nephritis, Hereditary / complications*
  • Nephritis, Hereditary / genetics
  • Nephritis, Hereditary / pathology
  • Pedigree