Hyperechogenic fetal bowel: counseling difficulties

Eur J Med Genet. 2005 Oct-Dec;48(4):421-5. doi: 10.1016/j.ejmg.2005.05.001.

Abstract

The detection of echodense fetal bowel on ultrasound examination in the second trimester of pregnancy justifies invasive procedures such as amniocentesis to detect an underlying cause. We present a case in which initial tests identified only one mutation in the cystic fibrosis transmembrane regulator (CFTR)-gene of the fetus, the family history being negative for CF. Strongly reduced intestinal enzyme activities suggested intestinal obstruction and further increased the estimated risk for CF. After the 24th gestational week, a second mutation was found, confirming cystic fibrosis in this child. Problems in counseling in this particular case are discussed.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Cystic Fibrosis / diagnosis*
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Female
  • Fetal Diseases / diagnostic imaging*
  • Fetus / abnormalities
  • Genetic Counseling*
  • Humans
  • Infant, Newborn
  • Intestines / embryology
  • Intestines / pathology*
  • Male
  • Pregnancy
  • Ultrasonography, Prenatal*

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator