Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutation

Pediatr Nephrol. 2012 Oct;27(10):1989-93. doi: 10.1007/s00467-012-2205-x. Epub 2012 Jun 4.

Abstract

Background: Renal coloboma syndrome (RCS) is a highly variable syndrome characterized by renal and ocular abnormalities. It is associated in about 50 % of cases with mutations of PAX2, a gene encoding a transcription factor required during development.

Case-diagnosis/treatment: The case study involves two monozygotic twin sisters with RCS showing highly discordant phenotypes. Twin 1 was antenatally diagnosed with multiple cysts in the right kidney. She had complicated vacuum-assisted delivery with acute renal failure. She developed proteinuria at age 4 years, followed by a progressive rise in serum creatinine requiring renal replacement therapy at age 22. No ocular abnormalities have been detected. Twin 2 experienced rapidly reversible acute renal failure without renal morphological abnormalities at birth. At age 2 years, complete visual acuity loss of the left eye secondary to an optic disc coloboma was diagnosed. No significant events occurred until the age of 20, when clinical proteinuria was detected. Proteinuria remission was obtained by multidrug treatment. In both patients, a novel de novo mutation of PAX2 was detected, which leads to the substitution of a highly conserved cysteine (p.C52Y).

Conclusions: The patients described provide an extreme example of clinical variability in RCS. The role of environmental, genetic, and epigenetic factors is discussed.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Child, Preschool
  • Coloboma / diagnosis
  • Coloboma / genetics*
  • Coloboma / therapy
  • Cysteine
  • Disease Progression
  • Diseases in Twins / diagnosis
  • Diseases in Twins / genetics*
  • Diseases in Twins / therapy
  • Environment
  • Female
  • Genetic Predisposition to Disease
  • Heterozygote
  • Humans
  • Mutation*
  • PAX2 Transcription Factor / genetics*
  • Phenotype
  • Renal Insufficiency / diagnosis
  • Renal Insufficiency / genetics*
  • Renal Insufficiency / therapy
  • Risk Factors
  • Twins, Monozygotic / genetics*
  • Vesico-Ureteral Reflux / diagnosis
  • Vesico-Ureteral Reflux / genetics*
  • Vesico-Ureteral Reflux / therapy
  • Young Adult

Substances

  • PAX2 Transcription Factor
  • PAX2 protein, human
  • Cysteine

Supplementary concepts

  • Papillorenal syndrome