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AJP Rep 2014; 4(01): 045-048
DOI: 10.1055/s-0034-1371750
Case Report
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

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

Katherine Jacobs
1   Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Women's Health, University of Minnesota, Minneapolis, Minnesota
,
Lauren Giacobbe
1   Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Women's Health, University of Minnesota, Minneapolis, Minnesota
,
Marijo Aguilera
1   Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Women's Health, University of Minnesota, Minneapolis, Minnesota
,
Kirk Ramin
1   Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Women's Health, University of Minnesota, Minneapolis, Minnesota
,
Shanthi Sivanandam
2   Division of Pediatric Cardiology, Amplatz Children's Hospital Heart Center, University of Minnesota, Minneapolis, Minnesota
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Publikationsverlauf

26. November 2013

07. Januar 2014

Publikationsdatum:
02. April 2014 (online)

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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.

Keywords

fetal - noncompaction cardiomyopathy - coarctation of the aorta
 

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