Genome-wide linkage scan for bladder exstrophy-epispadias complex

Michael Ludwig, Franz Rüschendorf, Kathrin Saar, Norbert Hübner, Lothar Siekmann, Simeon Boyd, Heiko Reutter

Research output: Contribution to journalArticle

16 Scopus citations

Abstract

BACKGROUND: The bladder exstrophy-epispadias complex represents a spectrum of urogenital anomalies in which part or all of the distal urinary tract fail to close and are exposed on the outer abdominal wall. Previous studies are suggestive of an underlying multifactorial mode of inheritance. However, no genetic or nongenetic factor has been identified so far. In this study, we sought risk loci by parametric and nonparametric linkage analysis, searching for homozygous segments, and more complex inherited loci, respectively. METHODS: Two pedigrees, Spanish and German, each comprising two members affected with classical bladder exstrophy, were analyzed by genome-wide linkage scan. RESULTS: Evidence for possible risk/modifying loci on chromosomes 2p22.1-p21, 2p25.2-p25.1, 4q23-q32.3, 7q21.3-q33, 7q34-q36.1, 14q31.1-q32.2, and 19q13.33-q13.43 (LOD scores >1.50) was obtained. CONCLUSIONS: This study was the first positional approach to identify chromosomal candidate regions causally related to bladder exstrophy-epispadias complex. Our results suggest the presence of susceptibility genes in the regions identified. These regions need to be confirmed in future studies.

Original languageEnglish (US)
Pages (from-to)174-178
Number of pages5
JournalBirth Defects Research Part A - Clinical and Molecular Teratology
Volume85
Issue number2
DOIs
StatePublished - Feb 2009

Keywords

  • Bladder exstrophy-epispadias complex
  • Epispadias
  • Exstrophy
  • Genome-wide linkage scan
  • Linkage analysis
  • SNP markers

ASJC Scopus subject areas

  • Developmental Biology
  • Pediatrics, Perinatology, and Child Health
  • Embryology

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