Non-compacted myocardium and foetal left isomerism as a hydrops’ aetiology
We present a case report of a pregnant woman with increased risk for trisomy 21 at first-trimester screening, assessed by ultrasonography, that was sent to our hospital. Amniocentesis was performed at 14 weeks and 2 days to obtain foetal karyotype that was normal (46,XX). At 19 weeks and 1 day, foet...
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| Veröffentlicht in: | Cardiology in the young 2010-04, Vol.20 (2), p.223-225 |
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| container_title | Cardiology in the young |
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| creator | Rocha, Ilda J. G. Nogueira, Rosete M. A. N. Carriço, Ana L. C. |
| description | We present a case report of a pregnant woman with increased risk for trisomy 21 at first-trimester screening, assessed by ultrasonography, that was sent to our hospital. Amniocentesis was performed at 14 weeks and 2 days to obtain foetal karyotype that was normal (46,XX). At 19 weeks and 1 day, foetal hydrops associated with cardiac malformation was detected by routine scan. Foetal echocardiogram revealed a complete auriculoventricular septal defect, non-compacted myocardium, and a bradycardia of 70–90 beats per minute, which lead to the suspicion of left isomerism. Foetal death occurred at 20 weeks and 3 days. Autopsy was consistent with the prenatal diagnosis. |
| doi_str_mv | 10.1017/S1047951110000144 |
| format | Article |
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| source | MEDLINE; Cambridge University Press Journals Complete |
| subjects | Adult Auriculoventricular septal defect cardiac malformation endocardial fibroelastosis Female Fetal Death Fetal Diseases - diagnostic imaging Heart Defects, Congenital - complications Humans Hydrops Fetalis - diagnostic imaging Hydrops Fetalis - etiology Isolated Noncompaction of the Ventricular Myocardium - diagnostic imaging Pregnancy Ultrasonography, Prenatal |
| title | Non-compacted myocardium and foetal left isomerism as a hydrops’ aetiology |
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