Prenatal cytogenetic diagnosis from fetal urine in lower urinary tract obstruction

Sina Haeri, Simone Hernandez Ruano, Leila M.S. Farah, Raquel Joffe, Rodrigo Ruano

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

The aim of this study was to test if prenatal cytogenetic diagnosis can be performed on fetal urine in fetal lower urinary tract obstruction. In this retrospective cohort study of fetuses with lower urinary tract obstruction (LUTO) over a 4-year period at one institution, cytogenetic evaluation was attempted on fetal urine samples as well as amniotic fluid specimens. A total of 11 cases, ranging in gestational age from 15 to 25 weeks, underwent amniocentesis and vesicocentesis. Traditional cytogenetic evaluation was successfully completed in amniotic fluid and fetal urine samples in all 11 cases (100%). The karyotype was normal in seven (64%), trisomy 21 in two (18%), Trisomy 13 in one (9%), and partial chromosome 4 deletion in one (9%). Traditional cytogenetic evaluation can be successfully performed on fetal urine samples in cases of lower urinary tract obstruction.

Original languageEnglish (US)
Pages (from-to)89-91
Number of pages3
JournalCongenital Anomalies
Volume53
Issue number2
DOIs
StatePublished - Jun 1 2013

Keywords

  • Fetal karyotype
  • Lower urinary tract obstruction
  • Posterior urethral valve
  • Urethral atresia
  • Vesicocentesis

ASJC Scopus subject areas

  • Medicine(all)

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