<?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>2709-7927</journal-id>
<journal-title><![CDATA[Acta Médica del Centro]]></journal-title>
<abbrev-journal-title><![CDATA[Acta méd centro]]></abbrev-journal-title>
<issn>2709-7927</issn>
<publisher>
<publisher-name><![CDATA[Hospital Provincial Clínico Quirúrgico Universitario Arnaldo Milián Castro]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2709-79272020000200237</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome 18q-. Informe de caso]]></article-title>
<article-title xml:lang="en"><![CDATA[18q- syndrome. Case report]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Morales Femenia]]></surname>
<given-names><![CDATA[Yurkina]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Alonso Gutiérrez]]></surname>
<given-names><![CDATA[Grisel María]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Santos González-Elías]]></surname>
<given-names><![CDATA[Carlos Angel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Universitario &#8220;Dr. Antonio Luaces Iraola&#8221;  ]]></institution>
<addr-line><![CDATA[Ciego de Ávila Ciego de Ávila]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2020</year>
</pub-date>
<volume>14</volume>
<numero>2</numero>
<fpage>237</fpage>
<lpage>242</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S2709-79272020000200237&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S2709-79272020000200237&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S2709-79272020000200237&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  el síndrome 18q- se considera una enfermedad rara y es el segundo síndrome más común que involucra al cromosoma 18. El propósito de este informe es describir las características y la estimulación del neurodesarrollo de un niño con deleción parcial del brazo largo del cromosoma 18 (18q-).  Información del paciente:  se presenta un niño de tres años de edad, masculino, con diagnóstico de un trastorno 18q-, que se encuentra en seguimiento por las Consultas de Logofoniatría y Neuropediatría de la Provincia Ciego de Ávila.  Conclusiones:  lo interesante de este caso es que dada la gran variabilidad fenotípica es muy difícil que dos niños con el síndrome 18q- presenten exactamente las mismas y tampoco todas las características fenotípicas propias de este síndrome; cada niño con este síndrome es único. Es fundamental e importante el diagnóstico precoz para mejorar la calidad de vida y estimular el neurodesarrollo de los niños con síndrome 18q-.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction:  syndrome 18q- is considered a rare disease and is the second most common syndrome that involves chromosome 18. The objective of this report is to describe the characteristics and stimulation of neurodevelopment of a child with partial deletion of the long arm of chromosome 18 (18q-).  Case report:  a three-year-old male boy is presented, with a diagnosis of an 18q- disorder, which is being followed up by the Logophoniatry and Neuropediatrics Consultations of the Ciego de Ávila Province.  Conclusions:  the interesting thing about this case is that due to the great phenotypic variability it is very difficult for two children with the 18q syndrome to have exactly the same and not all the phenotypic characteristics of this syndrome; Every child with this syndrome is unique. Early diagnosis is essential and important to improve the quality of life and stimulate neurodevelopment of children with 18q- syndrome.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[síndrome de deleción de 18q-]]></kwd>
<kwd lng="es"><![CDATA[deleción parcial 18q]]></kwd>
<kwd lng="es"><![CDATA[monosomía 18q]]></kwd>
<kwd lng="es"><![CDATA[síndrome de De Grouchy]]></kwd>
<kwd lng="es"><![CDATA[características]]></kwd>
<kwd lng="es"><![CDATA[estimulación del neurodesarrollo]]></kwd>
<kwd lng="en"><![CDATA[18q- deletion syndrome]]></kwd>
<kwd lng="en"><![CDATA[partial deletion 18q]]></kwd>
<kwd lng="en"><![CDATA[18q monosomy]]></kwd>
<kwd lng="en"><![CDATA[De Grouchy syndrome]]></kwd>
<kwd lng="en"><![CDATA[features]]></kwd>
<kwd lng="en"><![CDATA[neurodevelopmental stimulation]]></kwd>
</kwd-group>
</article-meta>
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