<?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>2664-3243</journal-id>
<journal-title><![CDATA[Vive Revista de Salud]]></journal-title>
<abbrev-journal-title><![CDATA[Vive Rev. Salud]]></abbrev-journal-title>
<issn>2664-3243</issn>
<publisher>
<publisher-name><![CDATA[CET-BOLIVIA]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2664-32432025000200781</article-id>
<article-id pub-id-type="doi">10.33996/revistavive.v8i23.411</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Anomalía de Ebstein: a propósito de un caso]]></article-title>
<article-title xml:lang="en"><![CDATA[Ebstein anomaly: a case report]]></article-title>
<article-title xml:lang="pt"><![CDATA[Anomalia de Ebstein: relato de caso]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Andrade Alban]]></surname>
<given-names><![CDATA[Noemí Rocío]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bombón Chico]]></surname>
<given-names><![CDATA[José Enrique]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cárdenas Verdezoto]]></surname>
<given-names><![CDATA[Sophia Beatriz]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Iglesias Espín]]></surname>
<given-names><![CDATA[Diana Sofía]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chuquimarca Salazar]]></surname>
<given-names><![CDATA[Cristian Santiago]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Curicama Gualli]]></surname>
<given-names><![CDATA[Marco Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Técnica de Ambato  ]]></institution>
<addr-line><![CDATA[Ambato ]]></addr-line>
<country>Ecuador</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2025</year>
</pub-date>
<volume>8</volume>
<numero>23</numero>
<fpage>781</fpage>
<lpage>789</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_arttext&amp;pid=S2664-32432025000200781&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_abstract&amp;pid=S2664-32432025000200781&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_pdf&amp;pid=S2664-32432025000200781&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN La anomalía de Ebstein es un defecto congénito complejo e infrecuente que incluye malformaciones morfofisiológicas de la válvula tricúspide y del ventrículo derecho, ocurre en 1 de cada 200 000 nacidos vivos y representa 1% de las cardiopatías congénitas, con frecuencia se relaciona con otros defectos como: tabique interauricular, estenosis o atresia pulmonar, comunicación interventricular, coartación aórtica y la tetralogía de Fallot. Paciente de 49 años con antecedente de anomalía de Ebstein e insuficiencia cardíaca congestiva refiere desde edad escolar presentar disnea de grandes esfuerzos, sin otra sintomatología acompañante, hace 15 días aproximadamente el cuadro se exacerba a disnea de medianos esfuerzos que se acompaña de palpitaciones, dolor torácico atípico y astenia, motivo por el cual se decide su ingreso. Ecocardiograma evidenció válvula tricúspide de implantación baja en el ventrículo derecho. Electrocardiograma reportó fibrilación auricular, bloqueo completo de rama derecha, trastorno de la repolarización ventricular. Paciente evoluciona favorablemente, no obstante, dadas las complicaciones propias de anomalía de Ebstein se decide tratamiento farmacológico expectante y paliativo. La anomalía de Ebstein representa una malformación cardíaca con una tasa de incidencia baja. La ecocardiografía se considera la modalidad preferida para detectar la patología debido a su capacidad para proporcionar una confirmación visual de la anomalía de la válvula tricúspide.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Ebstein's anomaly is a complex and rare congenital defect that includes morphophysiological malformations of the tricuspid valve and right ventricle. It occurs in 1 in 200,000 live births and represents 1% of congenital heart diseases. It is frequently associated with other defects such as: interatrial septum, pulmonary stenosis or atresia, ventricular septal defect, aortic coarctation, and tetralogy of Fallot. A 49-year-old patient with a history of Ebstein's anomaly and congestive heart failure reports dyspnea on heavy exertion since school age, without other accompanying symptoms. Approximately 15 days ago, the condition worsened to dyspnea on moderate exertion accompanied by palpitations, atypical chest pain, and asthenia, which is why the decision was made to admit him. An echocardiogram showed a low-set tricuspid valve in the right ventricle. An electrocardiogram revealed atrial fibrillation, complete right bundle branch block, and ventricular repolarization disorder. The patient is progressing favorably; however, given the complications associated with Ebstein's anomaly, expectant and palliative pharmacological treatment was decided upon. Ebstein's anomaly represents a cardiac malformation with a low incidence rate. Echocardiography is considered the preferred modality for detecting the disease due to its ability to provide visual confirmation of tricuspid valve abnormality.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[RESUMO A anomalia de Ebstein é um defeito congênito complexo e raro que inclui malformações morfofisiológicas da valva tricúspide e do ventrículo direito. Ocorre em 1 em cada 200.000 nascidos vivos e representa 1% das cardiopatias congênitas. É frequentemente associada a outros defeitos, como: septo interatrial, estenose ou atresia pulmonar, comunicação interventricular, coarctação aórtica e tetralogia de Fallot. Um paciente de 49 anos com histórico de anomalia de Ebstein e insuficiência cardíaca congestiva relata dispneia aos grandes esforços desde a idade escolar, sem outros sintomas associados. Há aproximadamente 15 dias, o quadro piorou para dispneia aos esforços moderados, acompanhada de palpitações, dor torácica atípica e astenia, razão pela qual foi tomada a decisão de interná-lo. Um ecocardiograma mostrou uma valva tricúspide de configuração baixa no ventrículo direito. Um eletrocardiograma revelou fibrilação atrial, bloqueio completo do ramo direito e distúrbio de repolarização ventricular. O paciente evolui favoravelmente; no entanto, dadas as complicações associadas à anomalia de Ebstein, optou-se por tratamento farmacológico expectante e paliativo. A anomalia de Ebstein representa uma malformação cardíaca com baixa taxa de incidência. A ecocardiografia é considerada a modalidade de escolha para a detecção da doença devido à sua capacidade de fornecer confirmação visual da anormalidade da valva tricúspide.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Anomalía de Ebstein]]></kwd>
<kwd lng="es"><![CDATA[Cardiopatías Congénitas]]></kwd>
<kwd lng="es"><![CDATA[Válvula Tricúspide]]></kwd>
<kwd lng="en"><![CDATA[Ebstein's anomaly]]></kwd>
<kwd lng="en"><![CDATA[Congenital heart disease]]></kwd>
<kwd lng="en"><![CDATA[Tricuspid valve]]></kwd>
<kwd lng="pt"><![CDATA[Anomalia de Ebstein]]></kwd>
<kwd lng="pt"><![CDATA[Cardiopatia congénita]]></kwd>
<kwd lng="pt"><![CDATA[Valva tricúspide]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Inzunza-Cervantes]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Herrera-Gavilanes]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Espinoza-Escobar]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Zazueta-Armenta]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Cortés-García]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Ornelas-Aguirre]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[[Ebstein&#8217;s anomaly with ventricular preexcitation in an adult patient].]]></article-title>
<source><![CDATA[Rev Medica Inst Mex Seguro Soc]]></source>
<year>2022</year>
<volume>60</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>466-73</page-range></nlm-citation>
</ref>
<ref id="B2">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Alves]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<name>
<surname><![CDATA[Lima]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Rasla]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ebstein&#8217;s Anomaly of the Tricuspid Valve.]]></article-title>
<source><![CDATA[R I Med J 2013]]></source>
<year>2024</year>
<volume>107</volume>
<numero>5</numero>
<issue>5</issue>
<page-range>21-4</page-range></nlm-citation>
</ref>
<ref id="B3">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Umar]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Zagga]]></surname>
<given-names><![CDATA[U]]></given-names>
</name>
<name>
<surname><![CDATA[Akintomide]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Maiyaki]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Umar]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Dankiri]]></surname>
<given-names><![CDATA[N,]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ebstein&#8217;s Anomaly: An Unanticipated Differential Diagnosis of Egg-on-Stick Appearance and the Diagnostic Dilemma.]]></article-title>
<source><![CDATA[Am J Case Rep]]></source>
<year>2021</year>
<volume>2</volume>
<page-range>2</page-range></nlm-citation>
</ref>
<ref id="B4">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Braga]]></surname>
<given-names><![CDATA[De Souza E]]></given-names>
</name>
<name>
<surname><![CDATA[Ramirez]]></surname>
<given-names><![CDATA[Vallejo E]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Reporte de caso clínico: Cardiopatía congénita cianótica con Anomalía de Ebstein, tipo B de Carpentier.]]></article-title>
<source><![CDATA[Cienc E Investig Medico Estud Latinoam]]></source>
<year>2021</year>
<volume>2</volume>
<page-range>6</page-range></nlm-citation>
</ref>
<ref id="B5">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Singh]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Hussain]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Horenstein]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Mahajan]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ebstein Anomaly and Malformation.]]></article-title>
<source><![CDATA[StatPearls]]></source>
<year>2024</year>
<volume>53482</volume>
<page-range>4</page-range><publisher-name><![CDATA[Treasure Island (FL): StatPearls Publishing]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B6">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Nartowicz]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Janus]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Ciep&#322;ucha]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Pyda]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Lesiak]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Trojnarska]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ebstein anomaly with severe tricuspid valve regurgitation: An unusual case of an 84-year natural course.]]></article-title>
<source><![CDATA[Pol Heart J]]></source>
<year>2024</year>
<volume>82</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>343-4</page-range></nlm-citation>
</ref>
<ref id="B7">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bautista-Vargas]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Anomalía de Ebstein y aneurisma del seno coronario.]]></article-title>
<source><![CDATA[Rev Colomb Cardiol]]></source>
<year>2022</year>
<volume>28</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>6367</page-range></nlm-citation>
</ref>
<ref id="B8">
<nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bessière]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Waldmann]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Combes]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Metton]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Dib]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Mondésert]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
</person-group>
<source><![CDATA[Ventricular Arrhythmias in Adults With Congenital Heart Disease, Part II. J Am Coll Cardiol.]]></source>
<year>2023</year>
<numero>11</numero>
<issue>11</issue>
</nlm-citation>
</ref>
<ref id="B9">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yu]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Yang]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Chen]]></surname>
<given-names><![CDATA[X]]></given-names>
</name>
<name>
<surname><![CDATA[Lu]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Zhao]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Yang]]></surname>
<given-names><![CDATA[S,]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Cardiac remodeling after tricuspid valve repair in Ebstein&#8217;s anomaly: a magnetic resonance study.]]></article-title>
<source><![CDATA[Eur Radiol]]></source>
<year>2022</year>
<volume>33</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>2052-61</page-range></nlm-citation>
</ref>
<ref id="B10">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pasqualin]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Boccellino]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Chessa]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Ciconte]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Marcolin]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Micaglio]]></surname>
<given-names><![CDATA[E,]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ebstein&#8217;s anomaly in children and adults: multidisciplinary insights into imaging and therapy.]]></article-title>
<source><![CDATA[Heart]]></source>
<year>2024</year>
<volume>110</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>235-44</page-range></nlm-citation>
</ref>
<ref id="B11">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vaikunth]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Lui]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Heart failure with reduced and preserved ejection fraction in adult congenital heart disease.]]></article-title>
<source><![CDATA[Heart Fail Rev]]></source>
<year>2020</year>
<volume>25</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>569-81</page-range></nlm-citation>
</ref>
<ref id="B12">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Buber]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Vatury]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Klempfner]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Tejman-Yarden]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[The impact of tricuspid valve regurgitation severity on exercise capacity and cardiac-related hospitalisations among adults with non-operated Ebstein&#8217;s anomaly.]]></article-title>
<source><![CDATA[Cardiol Young]]></source>
<year>2019</year>
<volume>29</volume>
<numero>6</numero>
<issue>6</issue>
<page-range>800-7</page-range></nlm-citation>
</ref>
<ref id="B13">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pérez&#8208;Riera]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Barbosa&#8208;Barros]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Daminello&#8208;Raimundo]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[De]]></surname>
<given-names><![CDATA[Abreu L]]></given-names>
</name>
<name>
<surname><![CDATA[Nikus]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Electro&#8208;vectorcardiographic and electrophysiological aspects of Ebstein&#8217;s anomaly.]]></article-title>
<source><![CDATA[Ann Noninvasive Electrocardiol]]></source>
<year>2019</year>
<volume>2</volume>
<page-range>4</page-range></nlm-citation>
</ref>
<ref id="B14">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Nguyen]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Nguyen]]></surname>
<given-names><![CDATA[X]]></given-names>
</name>
<name>
<surname><![CDATA[Pham]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Pham]]></surname>
<given-names><![CDATA[L. Successful Radiofrequency Ablation of the Right Lateral Accessory Pathway with Modified Carpentier Reconstruction Surgery in a Patient with Ebstein Anomaly Concomitant of Secundum Atrial Septal Defect]]></given-names>
</name>
<name>
<surname><![CDATA[Atrial]]></surname>
<given-names><![CDATA[Fibrillation]]></given-names>
</name>
<name>
<surname><![CDATA[and]]></surname>
<given-names><![CDATA[Wolff-Parkinson-White Syndrome]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Nakajima H, editor.]]></article-title>
<source><![CDATA[Case Rep Vasc Med]]></source>
<year>2022</year>
<volume>2022</volume>
<page-range>1-6</page-range></nlm-citation>
</ref>
<ref id="B15">
<nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Sainathan]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
</person-group>
<source><![CDATA[Ebstein&#8217;s anomaly: contemporary management strategies. J Thorac]]></source>
<year>2020</year>
<volume>12</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>1161-73</page-range></nlm-citation>
</ref>
<ref id="B16">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chambergo-Michilot]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Espinoza-Gutiérrez]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Gómez]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Tenorio-Quispe]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Válvula tricúspide displásica (Ebstein-like).]]></article-title>
<source><![CDATA[Rev Colomb Cardiol]]></source>
<year>2020</year>
<volume>27</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>303-6</page-range></nlm-citation>
</ref>
<ref id="B17">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Holst]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Connolly]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Dearani]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ebstein&#8217;s Anomaly.]]></article-title>
<source><![CDATA[Methodist DeBakey Cardiovasc J]]></source>
<year>2019</year>
<volume>15</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>138</page-range></nlm-citation>
</ref>
<ref id="B18">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pacheco]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Torres]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[Serrano]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Adulto con anomalía de ebstein.]]></article-title>
<source><![CDATA[Rev Fac Cienc Médicas Univ Cuenca]]></source>
<year>2020</year>
<volume>3</volume>
<page-range>8</page-range></nlm-citation>
</ref>
<ref id="B19">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cepeda-Rodrigo]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Comín-Colet]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[García-Quintana]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Sánchez]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Zamorano]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[González-Juanatey]]></surname>
<given-names><![CDATA[J. Abordaje terapéutico del paciente con insuficiencia cardiaca]]></given-names>
</name>
<name>
<surname><![CDATA[fracción]]></surname>
<given-names><![CDATA[de eyección reducida]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Papel del vericiguat.]]></article-title>
<source><![CDATA[Rev Esp Cardiol Supl]]></source>
<year>2022</year>
<volume>22</volume>
<page-range>23-9</page-range></nlm-citation>
</ref>
<ref id="B20">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[González-Juanatey]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Anguita-Sánchez]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Bayes-Genís]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Comín-Colet]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[García-Quintana]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Recio-Mayoral]]></surname>
<given-names><![CDATA[A,]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Vericiguat en insuficiencia cardíaca: de la evidencia científica a la práctica clínica.]]></article-title>
<source><![CDATA[Rev Clínica Esp]]></source>
<year>2022</year>
<volume>222</volume>
<numero>6</numero>
<issue>6</issue>
<page-range>359-69</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
