<?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>1029-3019</journal-id>
<journal-title><![CDATA[MEDISAN]]></journal-title>
<abbrev-journal-title><![CDATA[MEDISAN]]></abbrev-journal-title>
<issn>1029-3019</issn>
<publisher>
<publisher-name><![CDATA[Centro Provincial de Información de Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1029-30192022000500006</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Factores precondicionantes de secuelas en niños menores de 5 años de edad con tortícolis muscular congénita]]></article-title>
<article-title xml:lang="en"><![CDATA[Precondicionant factors of sequela in children under 5 years with congenital muscular wryneck]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández Dinza]]></surname>
<given-names><![CDATA[Pablo Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pérez Infante]]></surname>
<given-names><![CDATA[Yaimet]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Castro Correoso]]></surname>
<given-names><![CDATA[Vivianne]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Henriquez García]]></surname>
<given-names><![CDATA[Yanet]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Docente Pediátrico Sur Dr. Antonio María Béguez César  ]]></institution>
<addr-line><![CDATA[Santiago de Cuba ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de Ciencias Médicas Facultad de Estomatología ]]></institution>
<addr-line><![CDATA[Santiago de Cuba ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>10</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>10</month>
<year>2022</year>
</pub-date>
<volume>26</volume>
<numero>5</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1029-30192022000500006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1029-30192022000500006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1029-30192022000500006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  El espectro de secuelas de la tortícolis muscular congénita es amplio. Algunos niños con dichas secuelas requieren de costosas y complejas operaciones.  Objetivo:  Determinar los factores precondicionantes asociados a secuelas orgánicas de la tortícolis muscular congénita en pacientes desde un mes hasta 5 años de edad.  Métodos:  Se realizó un estudio retrospectivo, analítico, no experimental de casos y controles que incluyó a niños con diagnóstico de tortícolis muscular congénita, atendidos en la consulta de Neurodesarrollo del Hospital Infantil Antonio María Beguez César de Santiago de Cuba, desde enero del 2017 hasta diciembre del 2020. El grupo de casos quedó conformado por todos los pacientes con complicaciones orgánicas de la tortícolis muscular congénita (24 niños) y el de control, por quienes no presentaron dichas complicaciones (72), seleccionados mediante un muestreo aleatorio simple.  Resultados: El sexo masculino predominó en los pacientes con complicaciones (62,5 %). La plagiocefalia y la asimetría facial fueron las secuelas más frecuentes. La edad menor de 6 meses en el momento del diagnóstico de la entidad constituyó un factor protector (OR = 0,12; IC 95 %: 0,04-0,33; p=0,000); hubo asociación de las complicaciones con el parto distócico (OR = 0,36; IC 95 %: 0,13-1,01; p=0,049) y con la macrosomía fetal (OR = 5,7; IC 95 %: 1,44-22,2; p=0,014). También existió asociación altamente significativa de las complicaciones con la asimetría de ambos músculos esternocleidomastoideos (OR = 11,4; IC 95 %: 3,7-34,9; p=0,000) y con el inicio tardío del tratamiento (OR = 8,5; IC 95 %: 3,0-24,1; p=0,000).  Conclusiones:  El parto distócico, la macrosomía fetal, la asimetría entre ambos músculos esternocleidomastoideos y el inicio tardío del tratamiento rehabilitador incrementaron el riesgo de complicaciones en los integrantes de la casuística.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction:  The spectrum of sequela of the congenital muscular wryneck is wide. Some children with these sequela require expensive and complex operations.  Objective:  To determine the precondicionant factors associated with organic sequela of the congenital muscular wryneck in patients since one month to 5 years.  Methods:  A retrospective, analytic, non experimental of cases and controls study was carried out that included children with diagnosis of congenital muscular wryneck, assisted in the Neurodevelopment Service of Antonio María Beguez Cesar Children Hospital in Santiago de Cuba, from January, 2017 to December, 2020. The group of cases was conformed by all the patients with organic complications of the congenital muscular wryneck (24 children) and the control group, for those who didn't present these complications (72), selected by means of a simple random sampling.  Results:  The male sex prevailed in the patients with complications (62.5 %). The plagiocephaly and the facial asymmetry were the most frequent sequela. The age under 6 months in the moment of the diagnosis of the entity constituted a protective factor (OR = 0.12; IC 95 %: 0.04-0.33; p=0.000); there was association of the complications with the dystocic childbirth (OR = 0.36; IC 95 %: 0.13-1.01; p=0.049) and with the fetal macrosomia (OR = 5.7; IC 95 %: 1.44-22,2; p=0.014). There was also highly significant association of the complications with the asymmetry of both sternocleidomastoid muscles (OR = 11.4; IC 95 %: 3.7-34.9; p=0-000) and with the late beginning of the treatment (OR = 8.5; IC 95 %: 3.0-24.1; p=0.000).  Conclusions:  The dystocic childbirth, fetal macrosomia, asymmetry between both sternocleidomastoid muscles and the late beginning of the rehabilitative treatment increased the risk of complications in the members of the case material.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[niños]]></kwd>
<kwd lng="es"><![CDATA[tortícolis muscular congénita]]></kwd>
<kwd lng="es"><![CDATA[secuelas]]></kwd>
<kwd lng="es"><![CDATA[factores precondicionantes]]></kwd>
<kwd lng="es"><![CDATA[tratamiento precoz]]></kwd>
<kwd lng="en"><![CDATA[children]]></kwd>
<kwd lng="en"><![CDATA[congenital muscular wryneck]]></kwd>
<kwd lng="en"><![CDATA[sequela]]></kwd>
<kwd lng="en"><![CDATA[precondicionant factors]]></kwd>
<kwd lng="en"><![CDATA[early treatment]]></kwd>
</kwd-group>
</article-meta>
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