<?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>2393-6797</journal-id>
<journal-title><![CDATA[Revista Uruguaya de Medicina Interna ]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Urug. Med. Int.]]></abbrev-journal-title>
<issn>2393-6797</issn>
<publisher>
<publisher-name><![CDATA[Sociedad de Medicina Interna del Uruguay]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2393-67972018000200031</article-id>
<article-id pub-id-type="doi">10.26445/rmu.3.2.4</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Gangliopatía: a propósito de un caso]]></article-title>
<article-title xml:lang="en"><![CDATA[Gangliopathy: a case report]]></article-title>
<article-title xml:lang="pt"><![CDATA[Gangliopatia: relato de caso]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Favotto]]></surname>
<given-names><![CDATA[Raúl Rozada]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Tejera]]></surname>
<given-names><![CDATA[Jochen Hackembruch]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de la República Facultad de Medicina Departamento de Neurofisiología Clínica. Sección de Enfermedades Neuromusculares]]></institution>
<addr-line><![CDATA[Montevideo ]]></addr-line>
<country>Uruguay</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>07</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>07</month>
<year>2018</year>
</pub-date>
<volume>3</volume>
<numero>2</numero>
<fpage>31</fpage>
<lpage>37</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_arttext&amp;pid=S2393-67972018000200031&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_abstract&amp;pid=S2393-67972018000200031&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_pdf&amp;pid=S2393-67972018000200031&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen: Las ganglionopatías, corresponden a un grupo de patologías con afección del soma de la primera neurona sensitiva del ganglio de la raíz dorsal y del ganglio de Gasser. Hay dos categorías etiológicas principales, adquiridas y hereditarias, con un perfil clínico y evolutivo diferente. Las manifestaciones dependen del tipo de neurona comprometida, las de mayor tamaño (fibras A beta y delta) conducen la sensibilidad propioceptiva y su alteración se traduce como ataxia sensitiva. Las de menor tamaño (fibras C) conducen la sensibilidad termoalgésica y su alteración se traduce por dolor neuropático. El cuadro generalmente es difuso y dado por síntomas puramente sensitivos (apalestesia/hipopalestesia, ataxia sensitiva y/o dolor neuropático), arreflexia y sin deficit motor. La evolución temporal es variable. El perfil neurofisiológico se define por disminución de amplitudes o ausencia de potenciales de acción sensitivos nerviosos (SNAP) con distribución multifocal y potenciales de acción musculares compuestos (CMAP) conservados o con alteraciones leves. El pronóstico funcional generalmente es malo, con recuperación limitada. Presentaremos los aspectos clínicos y neurofisiológicos de una paciente evaluada en nuestro servicio.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: The ganglionopathies correspond to a group of pathologies with soma involvement of the first sensory neuron of the dorsal root ganglion and Gasser's ganglion. There are two main etiological categories, acquired and hereditary, with a different clinical and evolutionary profile. The manifestations depend on the type of compromised neuron, the larger ones (A beta and delta fibers) lead to proprioceptive sensitivity and its alteration is translated as sensory ataxia. The smaller ones (C fibers) lead to thermoalgesic sensitivity and their alteration is translated by neuropathic pain. The picture is generally diffuse, symmetric and given by purely sensitive symptoms (apalestesia/hipopalestesia, sensory ataxia and/or neuropathic pain), absent reflexes and without motor deficit. The temporal evolution it&#8217;s variable. The neurophysiological profile is defined by decreased amplitudes or absence of sensory nervous action potentials (SNAP) with multifocal distribution and conserved compound muscle action potentials (CMAP) or with slight alterations. Functional prognosis is generally poor, with limited recovery. We will present the clinical and neurophysiological aspects of a patient evaluated in our service.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo: As ganglionopatias correspondem a um grupo de patologias com envolvimento soma do primeiro neurônio sensitivo do gânglio da raiz dorsal e do gânglio de Gasser. Existem duas categorias etiológicas principais, adquiridas e hereditárias, com perfil clínico e evolutivo diferente. As manifestações dependem do tipo de neurônio envolvido, as maiores (A beta e fibras delta) levam à sensibilidade proprioceptiva e sua alteração é traduzida como ataxia sensorial. As menores (fibras C) levam à sensibilidade termoalgesica e sua alteração é traduzida por dor neuropática. O quadro é geralmente difuso e dado por sintomas puramente sensíveis (apalestesia / hipopalestesia, ataxia sensitiva e / ou dor neuropática), arreflexia e sem déficit motor. A evolução temporal é variável. O perfil neurofisiológico é definido por amplitudes diminuídas ou ausência de potenciais de ação sensorial nervosa (SNAP) com distribuição multifocal e potenciais de ação muscular compostos (PAMC) preservados ou com alterações leves. O prognóstico funcional é geralmente ruim, com recuperação limitada. Apresentaremos os aspectos clínicos e neurofisiológicos de um paciente avaliado em nosso serviço.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Ganglionopatía]]></kwd>
<kwd lng="es"><![CDATA[no largo dependiente]]></kwd>
<kwd lng="es"><![CDATA[multifocal.]]></kwd>
<kwd lng="en"><![CDATA[Ganglionopathies]]></kwd>
<kwd lng="en"><![CDATA[non large dependent]]></kwd>
<kwd lng="en"><![CDATA[multifocal]]></kwd>
<kwd lng="pt"><![CDATA[Ganglionopatia]]></kwd>
<kwd lng="pt"><![CDATA[não a longo prazo]]></kwd>
<kwd lng="pt"><![CDATA[multifocal]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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