<?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>0376-7892</journal-id>
<journal-title><![CDATA[Cirugía Plástica Ibero-Latinoamericana]]></journal-title>
<abbrev-journal-title><![CDATA[Cir. plást. iberolatinoam.]]></abbrev-journal-title>
<issn>0376-7892</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Española de Cirugía Plástica, Reparadora y Estética (SECPRE)]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0376-78922024000300014</article-id>
<article-id pub-id-type="doi">10.4321/s0376-78922024000300014</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Corrección de déficit de almohadillado palmar por amiotrofia distal de origen neurológico mediante lipoinfiltración. Caso clínico]]></article-title>
<article-title xml:lang="en"><![CDATA[Correction of soft tissue defects on the palm of the hand due to neurologic distal amyotrophy using lipofilling. Case report]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez-Fernández]]></surname>
<given-names><![CDATA[Fernando]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Salas-López]]></surname>
<given-names><![CDATA[Ainhoa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Peralta-Amores]]></surname>
<given-names><![CDATA[Francesc]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Beato-García-De Sola]]></surname>
<given-names><![CDATA[Paola]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Morgado-Águila]]></surname>
<given-names><![CDATA[Carolina]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Universitario de Cáceres  ]]></institution>
<addr-line><![CDATA[Cáceres ]]></addr-line>
<country>España</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Universitario de Bellvitge  ]]></institution>
<addr-line><![CDATA[Barcelona ]]></addr-line>
<country>España</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital Universitario de Cáceres  ]]></institution>
<addr-line><![CDATA[Cáceres ]]></addr-line>
<country>España</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2024</year>
</pub-date>
<volume>50</volume>
<numero>3</numero>
<fpage>341</fpage>
<lpage>346</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_arttext&amp;pid=S0376-78922024000300014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_abstract&amp;pid=S0376-78922024000300014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_pdf&amp;pid=S0376-78922024000300014&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen La enfermedad de Charcot-Marie-Tooth (CMT) consiste en un espectro de trastornos neuropáticos sensitivo-motores hereditarios primarios de origen genético que afectan al sistema nervioso periférico. Presentamos el caso de una paciente con enfermedad CMT tipo 1A de años de evolución con déficit de almohadillado palmar asociado a la amiotrofia distal propia de la enfermedad, lo cual ocasiona disfunción por dolor al apoyo palmar y al agarre. Fue tratada mediante lipoinfiltración de palmas de manos con buen resultado funcional y mejoría en la calidad de vida a largo plazo.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Charcot-Marie-Tooth (CMT) disease is a genetically transmitted illness which encompasses a range of primary hereditary neuropathic sensory-motor disturbances affecting peripheral nervous system. We present a patient suffering long-term CMT type 1A who presents a soft tissue defect on the padding of the palms of the hands associated with the characteristic distal amyotrophy due to the disease, which causes dysfunctional and painful gripping and resting of the palm of the hand against surfaces. Our patient was submitted to a lipofilling procedure on the palms of both hands resulting on a satisfactory functional outcome and a substantial improvement of long-term quality of life.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Lipofilling]]></kwd>
<kwd lng="en"><![CDATA[Autologous fat grafting]]></kwd>
<kwd lng="en"><![CDATA[Charcot-Marie-Tooth disease]]></kwd>
<kwd lng="en"><![CDATA[Distal amyotrophy]]></kwd>
<kwd lng="es"><![CDATA[Lipoinfiltración]]></kwd>
<kwd lng="es"><![CDATA[Injerto graso autólogo]]></kwd>
<kwd lng="es"><![CDATA[Enfermedad de Charcot-Marie-Tooth]]></kwd>
<kwd lng="es"><![CDATA[Amiotrofia distal]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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