1. A Case of Fetal Diagnosis of Noncompaction Cardiomyopathy and Coarctation of the Aorta
- Author
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Shanthi Sivanandam, Katherine Jacobs, Kirk D. Ramin, Lauren Giacobbe, and Marijo Aguilera
- Subjects
Noncompaction cardiomyopathy ,Pediatrics ,medicine.medical_specialty ,Population ,Coarctation of the aorta ,Cardiomyopathy ,lcsh:Gynecology and obstetrics ,Article ,Internal medicine ,medicine ,education ,lcsh:RG1-991 ,Fetus ,education.field_of_study ,business.industry ,Obstetrics and Gynecology ,noncompaction cardiomyopathy ,medicine.disease ,fetal ,Neonatal morbidity ,Pediatrics, Perinatology and Child Health ,Cardiology ,Gestation ,coarctation of the aorta ,Fetal diagnosis ,business - 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.
- Published
- 2014