<?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>0034-7531</journal-id>
<journal-title><![CDATA[Revista Cubana de Pediatría]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Cubana Pediatr]]></abbrev-journal-title>
<issn>0034-7531</issn>
<publisher>
<publisher-name><![CDATA[Centro Nacional de Información de Ciencias MédicasEditorial Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-75312018000400004</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Patrón clínico y epidemiológico de la atresia de vías biliares en Cuba]]></article-title>
<article-title xml:lang="en"><![CDATA[Clinical and epidemiological pattern of biliary atresia in Cuba]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Silverio García]]></surname>
<given-names><![CDATA[César Emilio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pérez Valencia]]></surname>
<given-names><![CDATA[Diana Cristina]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Villamil Martínez]]></surname>
<given-names><![CDATA[Ramón]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sosa Palacios]]></surname>
<given-names><![CDATA[Oramis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cobas Torres]]></surname>
<given-names><![CDATA[Yanisleidy]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Pediátrico Universitario &#8220;William Soler&#8221; Servicio de Hepatología ]]></institution>
<addr-line><![CDATA[La Habana ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Pediátrico Universitario &#8220;William Soler&#8221; Departamento de Pediatría ]]></institution>
<addr-line><![CDATA[La Habana ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital Pediátrico Universitario &#8220;William Soler&#8221; Servicio de Trasplante Hepático ]]></institution>
<addr-line><![CDATA[La Habana ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<volume>90</volume>
<numero>4</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S0034-75312018000400004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S0034-75312018000400004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S0034-75312018000400004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  La atresia de vías biliares es una colangiopatía infrecuente que se presenta en recién nacidos entre la segunda y cuarta semana de vida.  Objetivo:  Determinar el patrón clínico-epidemiológico de la atresia de vías biliares en Cuba.  Método:  Estudio descriptivo en la población con atresia de vías biliares(n= 30) atendida en el Hospital &#8220;William Soler&#8221; (enero 2011-diciembre 2015). Se midieron los rasgos clínicos, humorales y variables epidemiológicas con análisis de incidencia (por 1 000 nacidos vivos) y pruebas estadísticas con significación para p&lt;0,05).  Resultados:  La incidencia en Cuba es de 0,47x 10 000 nacidos vivos (1: 21 078 nacidos vivos), en Mayabeque, la más alta con 1: 6 784. Todos tuvieron ictericia y 96,7 % coluria. Se presentaron concentraciones elevadas de bilirrubina total (media= 184,9 µmol/L), ligera elevación de alaninoaminotransferasa (media= 201,8 U/L) y aspartatoaminotransferasa (media= 279,5 U/L), mayor aumento en la concentración de gammaglutamiltransferasa (media= 588 U/L) que de fosfatasa alcalina (media=1 557,1 u/L) e incremento del colesterol (6,8 mmol/L) con triglicéridos normales. El 70 % de los sometidos a intervención quirúrgica antes de los 60 días de nacido restablecieron el flujo biliar contra 35,5 % que no lo lograron cuando se intervinieron posteriormente.  Conclusiones:  La incidencia en la enfermedad en Cuba asciende, sin preferencia de género y es superior en Mayabeque. Son típicas las manifestaciones de ictericia, coluria, hiperbilirrubinemia, hipertransaminasemia ligera, hipercolesterolemia con alteración de gammaglutamiltransferasa más que de la fosfatasa alcalina y restablecimiento del flujo biliar en operados antes de los 60 días de nacido.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction:  Biliary atresia is an infrequent colangiopaty that it is present in newborns among the second and the forth weeks of life.  Objective: To determine the clinical and epidemiological pattern of biliary atresia in Cuba.  Method: Descriptive study in the population presenting biliary atresia (n= 30) attended in &#8220;William Soler&#8221; Hospital (from January, 2011 to December, 2015). Clinical and humoral features, and epidemiological variables were measured by an incidence analysis (per 1 000 live births) and statistical tests with significance of p&lt;0,05.  Results:  Incidence in Cuba is of 0.47 x 10 000 live births (1: 21 078 live births); in Mayabeque province, it is registered the highest incidence 1: 6 784. All the patients presented icterus and 96.7 % presented choluria. High concentrations of total bilirubine (mean= 184.9 µmol/L), slight increase of alaninoaminotransferasa (mean= 201.8 U/L) and aspartatoaminotransferasa (mean= 27.5 U/L) than in the alcaline fosfatase (mean= 1 557.1 U/L); and cholesterol increase (6.8 mmol/L) with normal triglycerides were present. 70 % of the patients that underwent surgeries before reaching 60 days of life could reestablish the biliar flow. 35 % did not achieve this while underwent a surgery after 60 days of life.  Conclusions: The incidence of this disease is increasing in Cuba, not having gender preferences and it is higher in Mayabeque province. Manifestations of icterus, choluria, hyperbilirubinemia, light hypertransaminasemia, hypercholesterolemia with gammaglutamiltransferasa alteration higher than alcaline fosfatase, and the reestablishment of the biliary flow in patients being operated before the 60 days of life, are common.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[atresia de vías biliares]]></kwd>
<kwd lng="es"><![CDATA[colangiopatía]]></kwd>
<kwd lng="es"><![CDATA[colestasis neonatal]]></kwd>
<kwd lng="es"><![CDATA[ictericia]]></kwd>
<kwd lng="en"><![CDATA[biliary atresia]]></kwd>
<kwd lng="en"><![CDATA[colangiopaty]]></kwd>
<kwd lng="en"><![CDATA[neonatal cholestasis]]></kwd>
<kwd lng="en"><![CDATA[icterus]]></kwd>
</kwd-group>
</article-meta>
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