Neonatal ascites in autosomal recessive polycystic kidney disease (ARPKD)

Galina Ling, Daniel Landau, Carsten Bergmann, Esther Maor, Baruch Yerushalmi

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Neonatal ascites is a rare entity, which is usually biliary, urinary, or chylous. Congenital hepatic fibrosis as part of the manifestations of autosomal recessive polycystic kidney disease (ARPKD) is usually a histological adjunct to the diagnosis of this mainly clinically renal entity in the neonatal period. Case-diagnosis: We describe a rare case of severe ascites in a newborn child complicating ARPKD, which was later confirmed by clinical, histological, and genetic studies. Conclusion: ARPKD should be considered in differential diagnosis of neonatal ascites.

Original languageEnglish
Pages (from-to)297-300
Number of pages4
JournalClinical Nephrology
Volume83
Issue number5
DOIs
StatePublished - 1 May 2015
Externally publishedYes

Keywords

  • ARPKD
  • Ascites
  • Congenital hepatic fibrosis
  • Neonate
  • SAAG

Fingerprint

Dive into the research topics of 'Neonatal ascites in autosomal recessive polycystic kidney disease (ARPKD)'. Together they form a unique fingerprint.

Cite this