<?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>0035-0052</journal-id>
<journal-title><![CDATA[Revista mexicana de pediatría]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. pediatr.]]></abbrev-journal-title>
<issn>0035-0052</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Pediatría A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0035-00522023000100017</article-id>
<article-id pub-id-type="doi">10.35366/112594</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Anomalía de prune-belly en un paciente con síndrome de Edwards]]></article-title>
<article-title xml:lang="en"><![CDATA[Prune-belly anomaly in a patient with Edwards syndrome]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ríos-Flores]]></surname>
<given-names><![CDATA[Izabel Marialexandra]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Corona-Rivera]]></surname>
<given-names><![CDATA[Alfredo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bobadilla-Morales]]></surname>
<given-names><![CDATA[Lucina]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Peña-Padilla]]></surname>
<given-names><![CDATA[Christian]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rocha-Castro]]></surname>
<given-names><![CDATA[Denys Vanessa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Corona-Rivera]]></surname>
<given-names><![CDATA[Jorge Román]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Civil de Guadalajara &#8220;Dr. Juan I. Menchaca&#8221; División de Pediatría Servicio de Genética y Unidad de Citogenética]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Departamento de Biología Molecular y Genómica Departamento de Biología Molecular y Genómica ]]></institution>
<addr-line><![CDATA[Guadalajara Jalisco]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>02</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>02</month>
<year>2023</year>
</pub-date>
<volume>90</volume>
<numero>1</numero>
<fpage>17</fpage>
<lpage>21</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0035-00522023000100017&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0035-00522023000100017&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0035-00522023000100017&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Introducción:  la anomalía de prune-belly (APB) se presenta raramente en fetos con trisomía 18 (T18).  Presentación del caso:  reportamos un RN masculino de 31 semanas con restricción del crecimiento intrauterino, polihidramnios, megavejiga y valvas uretrales posteriores. En la exploración física se identificó la APB y el fenotipo compatible con síndrome de Edwards; el paciente falleció horas después del nacimiento, pero se pudo comprobar el diagnóstico con cariotipo en sangre periférica: 47,XY,t(5;20)(q22;p11.2),t(8;18)(q22;q11.2),+18. Además, el análisis de microarreglos cromosómicos por aCGH: arr(18)x3, identificó traslocación recíproca doble, aparentemente balanceada.  Conclusiones:  los pacientes con T18 presentan múltiples malformaciones congénitas, pero su asociación con APB constituye algo atípico.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Introduction:  prune-belly anomaly (PBA) is rare in fetuses with trisomy 18 (T18).  Case presentation:  we report a 31-week-old male newborn with intrauterine growth restriction, polyhydramnios, megabladder, and posterior urethral valves. In the physical examination, the APB and the phenotype compatible with Edwards syndrome were identified. The patient died hours after birth, but the diagnosis could be confirmed by means of a peripheral blood karyotype: 47,XY,t(5;20)(q22;p11.2),t(8;18)(q22;q11.2),+18. Array comparative genomic hybridization (aCGH): arr(18)x3, indicated a double reciprocal translocation, apparently balanced.  Conclusions:  patients with T18 have multiple congenital malformations, but their association with APB is somewhat atypical.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[trisomía 18]]></kwd>
<kwd lng="es"><![CDATA[translocación recíproca doble]]></kwd>
<kwd lng="es"><![CDATA[anomalía de prune-belly]]></kwd>
<kwd lng="es"><![CDATA[megavejiga]]></kwd>
<kwd lng="es"><![CDATA[valvas uretrales posteriores]]></kwd>
<kwd lng="en"><![CDATA[trisomy 18]]></kwd>
<kwd lng="en"><![CDATA[double reciprocal translocation]]></kwd>
<kwd lng="en"><![CDATA[prune-belly anomaly]]></kwd>
<kwd lng="en"><![CDATA[megacystis]]></kwd>
<kwd lng="en"><![CDATA[posterior urethral valves]]></kwd>
</kwd-group>
</article-meta>
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