Human acardiac anomaly: a report of three cases

Eur J Obstet Gynecol Reprod Biol. 1991 Jan 4;38(1):79-85. doi: 10.1016/0028-2243(91)90212-4.

Abstract

We report on three cases of acardia, all of which had to be classified as acardius anceps. The degree of cardiac malformation ranged between a completely missing heart and a malrotation of a relatively well-developed heart. One fetus showed an intermediate form of cardiac malformation with a hypoplastic cor triloculare. Our findings suggest that the defect in cardiac development may take place at different times in early embryogenesis, resulting in differing degrees of cardiac malformation.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple
  • Abnormalities, Severe Teratoid*
  • Adult
  • Diseases in Twins*
  • Female
  • Fetal Death
  • Heart Defects, Congenital*
  • Humans
  • Pregnancy
  • Pregnancy, Multiple*