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	<title>EL FETO ACARDIO: UNA INTERESANTE VARIEDAD DE LA GEMELARIDAD. INFORME DE TRES CASOS. | Vila Bormey | Medicentro Electrónica</title>
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        <meta name="citation_author" content="Dra. Aimeé Vila Bormey"/>
        <meta name="citation_author" content="Dra. Nélida Sarasa Muñoz"/>
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	<a href="https://medicentro.sld.cu/index.php/medicentro/issue/view/9" target="_parent">Vol 2, No 1 (1998)</a> &gt;	<a href="https://medicentro.sld.cu/index.php/medicentro/article/view/25/0" class="current" target="_parent">Vila Bormey</a>
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	<div id="articleTitle"><h3>EL FETO ACARDIO: UNA INTERESANTE VARIEDAD DE LA GEMELARIDAD. INFORME DE TRES CASOS.</h3></div>
	<div id="authorString"><em>Dra. Aimeé Vila Bormey, Dra. Nélida Sarasa Muñoz, Dra. Irene Rodríguez Santos</em></div>

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		<div>Una de las más infrecuentes situaciones que se presenta en los embarazos gemelares es que uno de los gemelos sea "normal" y el otro carezca de un corazón funcionante. Esta rara entidad sólo se presenta en gestaciones múltiples monocigóticas. La supervivencia intraútero de tales malformados es posible debido a la comunicación con los vasos sanguíneos de su cogemelo, con el que se establece el conocido fenómeno de transfusión feto-fetal que crea una desigual irrigación sanguínea de los gemelos. El menos favorecido deviene en un monstruo acardio<sup>1,2</sup>.</div>

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