Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney disease

Daniel Landau, Hanna Shalev, Hanna Shulman, Yehiel Barki, Esther Maor, Ehud Zmora

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Two newborns with glomerulocystic kidney disease manifesting as late onset oligohydramnion and neonatal anuria, yet without severe respiratory distress, are presented. They had a similar perinatal course and associated clinical manifestations. No associated congenital or inherited malformation syndrome could be defined. Both infants' parents were first degree cousins and belonged to the same small Bedouin tribe, and neither they nor the infants' siblings had polycystic kidneys or renal insufficiency, pointing to either a possible genetic etiology or a common external toxic exposure.

Original languageEnglish
Pages (from-to)319-321
Number of pages3
JournalPediatric Nephrology
Volume14
Issue number4
DOIs
StatePublished - 1 Jan 2000

Keywords

  • Genetics
  • Glomerulocystic kidney disease
  • Oligohydramnion
  • Renal failure-neonate

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