American Journal of Perinatology Reports (Apr 2014)

A Case of Fetal Diagnosis of Noncompaction Cardiomyopathy and Coarctation of the Aorta

  • Katherine Jacobs,
  • Lauren Giacobbe,
  • Marijo Aguilera,
  • Kirk Ramin,
  • Shanthi Sivanandam

DOI
https://doi.org/10.1055/s-0034-1371750
Journal volume & issue
Vol. 4, no. 01
pp. 045 – 048

Abstract

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Abstract Background Left ventricular noncompaction (LVNC) cardiomyopathy is a rare form of cardiomyopathy. It is difficult to diagnose prenatally and therefore not well described in the fetal population. There have been a few reports in the literature detailing isolated cases of fetal and neonatal LVNC cardiomyopathy. Case Report We present a case of LVNC cardiomyopathy and coarctation of the aorta detected prenatally at 29 + 6 weeks of gestation with survival in infancy. This is the first case report in the literature describing the fetal diagnosis of noncompaction cardiomyopathy and associated coarctation of the aorta; a rare combination. Conclusion With a high index of suspicion, the antenatal diagnosis of noncompaction cardiomyopathy may improve neonatal morbidity and mortality.

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