<?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>0035-0052</journal-id>
<journal-title><![CDATA[Revista mexicana de pediatría]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. pediatr.]]></abbrev-journal-title>
<issn>0035-0052</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Pediatría A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0035-00522021000400149</article-id>
<article-id pub-id-type="doi">10.35366/102779</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de Miller Fisher: una variante poco común de Guillain Barré]]></article-title>
<article-title xml:lang="en"><![CDATA[Miller Fisher Syndrome: An uncommon Guillain Barré variant]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Morales-Galindo]]></surname>
<given-names><![CDATA[Ana Leticia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bolaños-Aparicio]]></surname>
<given-names><![CDATA[Luis Fernando]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Servicio de Pediatría  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto Mexicano del Seguro Social Centro Médico Nacional Siglo XXI Hospital de Pediatría]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<volume>88</volume>
<numero>4</numero>
<fpage>149</fpage>
<lpage>151</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0035-00522021000400149&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0035-00522021000400149&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0035-00522021000400149&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Objetivo:  Presentar el caso clínico de un paciente de 10 años con diagnóstico de síndrome de Miller Fisher, variante del síndrome de Guillain Barré, lo cual es raro en niños.  Descripción del caso:  Acude con oftalmoplejía, diplopía, debilidad muscular y ataxia; el diagnóstico de síndrome de Miller Fisher se realizó con base en los datos clínicos, presencia de disociación albúmino-citológica en el líquido cefalorraquídeo, y por el reporte de estudio electroneurográfico con neuroconducción motora anormal y polirradiculoneuropatía de tipo axonal. El paciente recibió gammaglobulina inmune intravenosa con lo que mostró mejoría de la sintomatología.  Conclusión:  El cuadro clínico debe orientar a la sospecha de síndrome de Miller Fisher, pero se deberán realizar estudios para establecer el diagnóstico y ofrecer tratamiento lo más pronto posible.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Objective:  We present the clinical case of a 10-year-old patient with a diagnosis of Miller Fisher syndrome, a variant of Guillain Barré syndrome, which is rare in children.  Case description:  Ophthalmoplegia, diplopia, muscle weakness, and ataxia was the patient&#8217;s clinical picture. Diagnosis of Miller Fisher syndrome was made based on the clinical data, the presence of albumin-cytological dissociation in the cerebrospinal fluid, and the report of an electroneurographic study with abnormal motor neuronconduction and polyradiculoneuropathy of the axonal type. The patient received intravenous immune gamma globulin showing improvement in symptoms.  Conclusion:  The clinical picture should guide the suspicion of Miller Fisher syndrome, but studies should be carried out to confirm the diagnosis, in order to offer treatment as soon as possible.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Miller Fisher]]></kwd>
<kwd lng="es"><![CDATA[Guillain Barré]]></kwd>
<kwd lng="es"><![CDATA[oftalmoplejía]]></kwd>
<kwd lng="es"><![CDATA[ataxia]]></kwd>
<kwd lng="es"><![CDATA[polirradiculoneuropatía]]></kwd>
<kwd lng="es"><![CDATA[neuroconducción]]></kwd>
<kwd lng="en"><![CDATA[Miller Fisher]]></kwd>
<kwd lng="en"><![CDATA[Guillain Barré]]></kwd>
<kwd lng="en"><![CDATA[ophthalmoplegia]]></kwd>
<kwd lng="en"><![CDATA[ataxia]]></kwd>
<kwd lng="en"><![CDATA[poly-radiculoneuropathy]]></kwd>
<kwd lng="en"><![CDATA[neuroconduction]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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