Abstract
Double inlet left ventricle as a rare cardiac malformation comprises a broad spectrum of anatomic variants making its correct antenatal diagnosis challenging. We report on echocardiographic findings of three fetuses found to have a less frequent morphologic subgroup of double inlet left ventricle, namely Holmes heart, characterized by a single (left) ventricle connected to both atrioventricular orifices and normally related arteries. We addressed the pre- and perinatal management as well as additional abnormalities and discussed our experiences together with what is known from current literature.
| Original language | English |
|---|---|
| Journal | Congenital Heart Disease |
| Volume | 8 |
| Issue number | 6 |
| Pages (from-to) | 579-584 |
| Number of pages | 6 |
| ISSN | 1747-079X |
| DOIs | |
| Publication status | Published - 01.11.2013 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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