<?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>0186-2391</journal-id>
<journal-title><![CDATA[Acta pediátrica de México]]></journal-title>
<abbrev-journal-title><![CDATA[Acta pediatr. Méx]]></abbrev-journal-title>
<issn>0186-2391</issn>
<publisher>
<publisher-name><![CDATA[Instituto Nacional de Pediatría]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0186-23912016000400215</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de Haddad: reporte de un caso y revisión de literatura]]></article-title>
<article-title xml:lang="en"><![CDATA[Haddad syndrome: a case report and literature review]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Santellán-Hernández]]></surname>
<given-names><![CDATA[JO]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Autónoma de Puebla  ]]></institution>
<addr-line><![CDATA[ Puebla]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2016</year>
</pub-date>
<volume>37</volume>
<numero>4</numero>
<fpage>215</fpage>
<lpage>221</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0186-23912016000400215&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0186-23912016000400215&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0186-23912016000400215&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen: El síndrome de Haddad es una enfermedad de origen genético, de transmisión autosómica dominante, resultado de una mutación en los genes que regulan la migración y diferenciación de las células de la cresta neural durante la gestación. Los niños con síndrome de Haddad inician con hipoxia que se desarrolla en las primeras horas de nacimiento y problemas del tránsito intestinal en los días subsecuentes. El diagnóstico debe realizarse por integración de las manifestaciones clínicas y la confirmación por análisis molecular del gen PHOX2B. El tratamiento de los niños con síndrome de Haddad está enfocado en proveer un adecuado control de la hipoxia por medio de ventilación mecánica asistida de por vida, colostomía o cirugía selectiva del colon, monitorización continua de signos vitales y saturación de oxígeno; mantener la profilaxis de enfermedades concomitantes como neumonía.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: Haddad syndrome is a genetic disease with autosomal dominant transmission result of a mutation in the genes that regulate migration and differentiation of neural crest cells during pregnancy. Children with Haddad syndrome begin with hypoxia that develops in the first few hours of birth and intestinal transit problems in the subsequent days. Diagnosis should be made by integrating the clinical manifestations and confirmation by genetic analysis of the gene PHOX2B. The treatment of children with Haddad syndrome is focused on providing adequate control of hypoxia through mechanical ventilation for life, colostomy or colon selective surgery, continuous monitoring of vital signs and oxygen saturation and maintain the prophylaxis for comorbidities as pneumonia.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[síndrome Haddad]]></kwd>
<kwd lng="es"><![CDATA[ondina]]></kwd>
<kwd lng="es"><![CDATA[Hirschsprung]]></kwd>
<kwd lng="es"><![CDATA[ciliopatía]]></kwd>
<kwd lng="es"><![CDATA[neurocristopatía]]></kwd>
<kwd lng="es"><![CDATA[ausencia de automatismo respiratorio]]></kwd>
<kwd lng="es"><![CDATA[gen PHOX2B]]></kwd>
<kwd lng="en"><![CDATA[Haddad syndrome]]></kwd>
<kwd lng="en"><![CDATA[ondina]]></kwd>
<kwd lng="en"><![CDATA[Hirschsprung]]></kwd>
<kwd lng="en"><![CDATA[ciliopathy]]></kwd>
<kwd lng="en"><![CDATA[neurocristopathy absence of respiratory automatism]]></kwd>
<kwd lng="en"><![CDATA[PHOX2B gene]]></kwd>
</kwd-group>
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