<?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>1870-7203</journal-id>
<journal-title><![CDATA[Acta médica Grupo Ángeles]]></journal-title>
<abbrev-journal-title><![CDATA[Acta méd. Grupo Ángeles]]></abbrev-journal-title>
<issn>1870-7203</issn>
<publisher>
<publisher-name><![CDATA[Grupo Ángeles, Servicios de Salud]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-72032017000100032</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Alta sospecha de enfermedades metabólicas congénitas en la población de ascendencia judía del Hospital Ángeles Lomas]]></article-title>
<article-title xml:lang="en"><![CDATA[High suspicion of congenital metabolic diseases in the population of Jewish descent of Hospital Ángeles Lomas]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Medina Doria]]></surname>
<given-names><![CDATA[Ana Carolina]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Oldak Kovalsky]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vela Amieva]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ibarra González]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fernández Lainez]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Oldak Skvirsky]]></surname>
<given-names><![CDATA[David]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Ángeles Lomas  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Anáhuac Hospital de la Beneficencia Española de la Laguna ]]></institution>
<addr-line><![CDATA[Norte ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Instituto Nacional de Pediatría  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,UNAM Instituto de Investigaciones Biomédicas ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Hospital Ángeles Lomas  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>02</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>02</month>
<year>2017</year>
</pub-date>
<volume>15</volume>
<numero>1</numero>
<fpage>32</fpage>
<lpage>35</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-72032017000100032&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-72032017000100032&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-72032017000100032&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Antecedentes:  La aplicación del tamiz neonatal y su ampliación a diversas enfermedades previamente no identificas por este método constituye un reto que ha dado pie a la aplicación de tecnologías como la plataforma múltiple y la espectrometría de masas en tándem. Se ha reconocido predisposición a dichas patologías en comunidades no estudiadas con anterioridad, como la judía. Su estudio es necesario para la identificación oportuna de dichos padecimientos.  Objetivo:  Reportar el número de tamices neonatales sospechosos de enfermedades metabólicas congénitas dentro de la población de ascendencia judía del Hospital Ángeles Lomas, comparado con el resto de la población.  Material y métodos:  Se analizaron todos los tamices neonatales realizados entre enero de 2010 y diciembre de 2014 en el Hospital Ángeles Lomas. Los resultados se consignaron en una base de datos exprofeso tomando los casos sospechosos, analizando el sexo y la etnicidad.  Resultados:  Se registraron 4,749 tamices metabólicos; 1,425 de padres judíos. Fueron sospechosos 172 tamices; de estos, 27 fueron consistentes en la segunda muestra. De estos últimos, 50% eran mujeres y 41% eran hombres, ambos judíos.  Conclusión:  Se observó una elevada sospecha de enfermedades congénitas dentro de la población de ascendencia judía, especialmente en G6PD y MCADD.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Background: The application of the neonatal screening and its extension to diseases not identified by the classic method constitutes a challenge that has led to the application of new technologies, such as the multiple platform and the tandem mass spectrometry. A predisposition to these pathologies has been identified in certain communities not previously studied, like the Jewish one; this makes their study essential for their timely diagnosis.  Objective:  To report the number of neonatal screening assays with suspicious reports for a congenital metabolic disease in those patients of Jewish ascent in the Angeles Lomas Hospital, and to compare it to the rest of the cases.  Material and methods: We analyzed all the neonatal screenings performed between January 2010 and December 2014 at the Angeles Lomas Hospital. The suspicious results were recorded in a database, analyzing sex and ethnicity.  Results:  4,749 neonatal screenings were analyzed; 1,425 were of Jewish ascendant. One hundred seventy-two screenings were suspicious, but only 27 were consistent in the second test. Of them, 50% of the females and 41% of the males were Jewish.  Conclusion: We observed an elevated incidence of suspicious cases of congenital diseases in population with Jewish ancestry, especially for G6PD and MCADD.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Tamiz neonatal]]></kwd>
<kwd lng="es"><![CDATA[enfermedades congénitas hereditarias]]></kwd>
<kwd lng="es"><![CDATA[población judía]]></kwd>
<kwd lng="en"><![CDATA[Neonatal screening]]></kwd>
<kwd lng="en"><![CDATA[congenital hereditary diseases]]></kwd>
<kwd lng="en"><![CDATA[Jewish population]]></kwd>
</kwd-group>
</article-meta>
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<given-names><![CDATA[JC]]></given-names>
</name>
<name>
<surname><![CDATA[Zakharia]]></surname>
<given-names><![CDATA[F]]></given-names>
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<name>
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<name>
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</person-group>
<source><![CDATA[Science]]></source>
<year>2014</year>
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</article>
