<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1028-9933</journal-id>
<journal-title><![CDATA[Revista Información Científica]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. inf. cient.]]></abbrev-journal-title>
<issn>1028-9933</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas Guantánamo]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1028-99332018000300643</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Anomalía de Ebstein en diagnóstico prenatal]]></article-title>
<article-title xml:lang="en"><![CDATA[Ebstein's anomaly in prenatal diagnosis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chibas Lamoth]]></surname>
<given-names><![CDATA[Yurima]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Marsillí Rivera]]></surname>
<given-names><![CDATA[Arismelis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez Ramírez]]></surname>
<given-names><![CDATA[Elsa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Policlínico Universitario &#8220;Emilio Daudinot Bueno&#8221;  ]]></institution>
<addr-line><![CDATA[ Guantánamo]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2018</year>
</pub-date>
<volume>97</volume>
<numero>3</numero>
<fpage>643</fpage>
<lpage>651</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1028-99332018000300643&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1028-99332018000300643&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1028-99332018000300643&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN Se presentó una gestante de 26 años de edad, mestiza, con antecedente de salud aparente evaluada en consulta de asesoramiento genético comunitaria con riesgo incrementado por exposición a teratógenos y mutágenos, que en la ecografía fetal del segundo trimestre se identificaron alteraciones cardiovasculares que pudieron estar relacionadas con anomalía de Ebstein. Este diagnóstico fue confirmado en el Centro Provincial de Genética Médica de Guantánamo y, posteriormente, en Santiago de Cuba. A pesar de ser una cardiopatía congénita poco frecuente, se consideraron: la intensificación de las acciones en la atención prenatal precoz de las gestantes en la comunidad, la realización y cumplimiento de los programas prenatales existentes en nuestro país, principalmente los ultrasonidos prenatales que continúan siendo el examen complementario de elección y ofrecer el asesoramiento genético específico en las familias afectadas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT A 26-year-old mixed-race pregnant woman with a history of apparent health evaluated in a community genetic counseling clinic with increased risk due to exposure to teratogens and mutagens was presented. Fetal echography of the second trimester identified cardiovascular alterations that may have been related to Ebstein's anomaly. Diagnosis that was confirmed in the Provincial Center of Medical Genetics of Guantanamo later was confirmed in Santiago de Cuba. Despite being a rare congenital heart disease, the following were considered: the intensification of the actions in the prenatal care of pregnant women in the community, the realization and fulfillment of the prenatal programs existing in our country, mainly the prenatal ultrasounds that continue being the complementary examination of choice and offer specific genetic counseling in affected families.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[anomalía de Ebstein]]></kwd>
<kwd lng="es"><![CDATA[malformaciones congénitas]]></kwd>
<kwd lng="es"><![CDATA[síndrome genético]]></kwd>
<kwd lng="en"><![CDATA[Ebstein´s anomaly]]></kwd>
<kwd lng="en"><![CDATA[congenital malformations]]></kwd>
<kwd lng="en"><![CDATA[genetic syndrome]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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