<?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>1029-3043</journal-id>
<journal-title><![CDATA[Medicentro Electrónica]]></journal-title>
<abbrev-journal-title><![CDATA[Medicentro Electrónica]]></abbrev-journal-title>
<issn>1029-3043</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas de Villa Clara]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1029-30432021000400670</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Enfoque médico social de la enfermedad renal crónica en Pediatría]]></article-title>
<article-title xml:lang="en"><![CDATA[Medical and social approach to chronic kidney disease in Paediatrics]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Saura Hernández]]></surname>
<given-names><![CDATA[María del Carmen]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Duménigo Lugo]]></surname>
<given-names><![CDATA[Dilayda]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gómez Milián]]></surname>
<given-names><![CDATA[Tania Mercy]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Pediátrico Universitario José Luis Miranda  ]]></institution>
<addr-line><![CDATA[Santa Clara Villa Clara]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2021</year>
</pub-date>
<volume>25</volume>
<numero>4</numero>
<fpage>670</fpage>
<lpage>690</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1029-30432021000400670&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1029-30432021000400670&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1029-30432021000400670&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  las malformaciones congénitas renales y de las vías urinarias constituyen un grupo heterogéneo de anomalías secundarias a un proceso anormal en el desarrollo embrionario del sistema renal.  Objetivo:  profundizar en los aspectos relacionados con el diagnóstico precoz de las malformaciones congénitas renales y de vías urinarias, como causa frecuente de la enfermedad renal crónica oculta en la edad pediátrica, desde una perspectiva integral y personalizada, sobre la base de un enfoque médico social.  Métodos:  se realizó una revisión sistemática sobre el tema en las bases de datos: EBSCO, SciELO, Scopus, PubMed, y en revistas de Nefrología pediátrica, de Pediatría, de Genética y de Teratología. Los artículos fueron publicados en idioma español o inglés. Se realizó un análisis de contenido directo para lograr la actualización teórica del tema con un enfoque médico social.  Conclusiones:  el desarrollo de la Nefrología pediátrica constituye una línea de trabajo del MINSAP. Sus principios son: la intersectorialidad, la prevención y la participación de especialidades afines (de manera que se alcancen resultados asistenciales, docentes e investigativos que determinen mayor calidad en el diagnóstico precoz de las malformaciones congénitas renales y de vías urinarias). Dicha afección es causa frecuente de la enfermedad renal crónica oculta en la edad pediátrica, desde una perspectiva integral y personalizada, sobre la base de un enfoque médico social.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction:  congenital renal and urinary tract malformations constitute a heterogeneous group of anomalies secondary to an abnormal embryonic development of the renal system.  Objective:  to study in depth the aspects related to the early diagnosis of congenital renal and urinary tract malformations, as a frequent cause of occult chronic kidney disease in the paediatric age group, from an integral and personalized perspective, based on a medical and social approach.  Methods:  a systematic review on the subject was carried out in the following databases: EBSCO, SciELO, Scopus, PubMed, and in journals of Paediatric Nephrology, Paediatrics, Genetics and Teratology. The articles were published in Spanish or English languages. A direct content analysis was performed to achieve the theoretical update of the topic with a medical and social approach.  Conclusions:  the development of Paediatric Nephrology constitutes a line of work of MINSAP. Its principles are intersectoriality, prevention and participation of related specialities (in order to achieve care, teaching and research results that determine greater quality in the early diagnosis of congenital renal and urinary tract malformations). This condition is a frequent cause of occult chronic kidney disease in the paediatric age group, from an integral and personalized perspective, based on a medical and social approach.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[diagnóstico prenatal]]></kwd>
<kwd lng="es"><![CDATA[anomalías congénitas]]></kwd>
<kwd lng="es"><![CDATA[sistema urinario/anomalías]]></kwd>
<kwd lng="es"><![CDATA[insuficiencia renal crónica/etiología]]></kwd>
<kwd lng="es"><![CDATA[proceso salud-enfermedad]]></kwd>
<kwd lng="en"><![CDATA[prenatal diagnosis]]></kwd>
<kwd lng="en"><![CDATA[congenital abnormalities]]></kwd>
<kwd lng="en"><![CDATA[urinary tract/abnormalities]]></kwd>
<kwd lng="en"><![CDATA[renal insufficiency, chronic/etiology]]></kwd>
<kwd lng="en"><![CDATA[health-disease process]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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