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

    ASJC Scopus subject areas

    • Pediatrics, Perinatology, and Child Health
    • Nephrology

    Fingerprint

    Dive into the research topics of 'Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney disease'. Together they form a unique fingerprint.

    Cite this