Prenatal diagnosis of supernumerary chromosome derivative (22) due to maternal balanced translocation in association with diaphragmatic hernia: a case report

Prenat Diagn. 1997 Aug;17(8):761-4.

Abstract

An aneuploid fetus was detected prenatally by cordocentesis at 27 weeks' gestation following ultrasonographic diagnosis of severe fetal growth retardation and a large diaphragmatic hernia. The fetal karyotype was revealed to be 47,XX,der(22)t(11;22)(q23.3;q11.2) after parental bloods confirmed a balanced reciprocal translocation in the mother. Approximately 85 cases with an unbalanced karyotype 47,XX(or XY),+der(22),t(11;22) due to 3:1 meiotic disjunction in the parental translocation carrier have been reported in the world literature and only one of them was diagnosed prenatally. This is the first detailed case report of a supernumerary derivative (22) chromosome abnormality diagnosed prenatally in association with diaphragmatic hernia.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 22*
  • Cordocentesis*
  • Female
  • Fetal Growth Retardation / diagnostic imaging
  • Hernia, Diaphragmatic / diagnosis
  • Hernia, Diaphragmatic / genetics*
  • Humans
  • Karyotyping
  • Mothers
  • Pregnancy
  • Translocation, Genetic*
  • Ultrasonography, Prenatal*