Clinical and pathological features of a neonate with autosomal recessive polycystic kidney disease caused by a nonsense PKHD1 mutation

World J Pediatr. 2013 Feb;9(1):76-9. doi: 10.1007/s12519-013-0407-3. Epub 2013 Feb 7.

Abstract

Background: Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary nephropathies in childhood. We report a neonate with ARPKD presenting with oligohydramnios, enlargement and increased echogenicity of both kidneys shown by antenatal sonograms after a 29-week gestation and died within the first few hours of life.

Methods: The neonate was investigated pathologically post-mortem. PCR-DNA direct sequencing was performed to detect the exons of the PKHD1 gene for mutation analysis.

Results: Autopsy findings of the kidney and liver confirmed the diagnostic hypothesis. PKHD1 mutation analysis revealed that there was a homozygous nonsense mutation c.9319C>T (p.R3107X), which was found to be pathogenic, in exon 58 in the neonate.

Conclusions: The recurrence of PKHD1 mutation c.9319C>T (p.R3107X) in the ARPKD population might be a good evidence that it is disease associated. Given the limitations of antenatal ultrasound, PKHD1 mutation analysis is helpful for accurate genetic counseling and early prenatal diagnosis.

Publication types

  • Case Reports

MeSH terms

  • Codon, Nonsense*
  • Fatal Outcome
  • Humans
  • Infant, Newborn
  • Male
  • Mutation*
  • Polycystic Kidney, Autosomal Recessive / diagnosis*
  • Polycystic Kidney, Autosomal Recessive / genetics*
  • Polycystic Kidney, Autosomal Recessive / pathology
  • Receptors, Cell Surface / genetics*

Substances

  • Codon, Nonsense
  • PKHD1 protein, human
  • Receptors, Cell Surface