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Síndrome Linfedema-Distiquiasis
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"apellidos" => "Soriano Belmonte" ] ] ] ] ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403307703764?idApp=UINPBA00005H" "url" => "/16954033/0000006600000002/v2_201308271339/S1695403307703764/v2_201308271339/es/main.assets" ] "es" => array:10 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Pósters</span>" "titulo" => "Síndrome Linfedema-Distiquiasis" "tieneTextoCompleto" => 0 "paginas" => array:1 [ 0 => array:1 [ "paginaInicial" => "221" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "C. Iglesias Blázquez, T. del Rosal Rabes, E.P. Gutiérrez González, J. Casas Rivero, J.M. Marugán de Miguelsanz" "autores" => array:5 [ 0 => array:3 [ "nombre" => "C." "apellidos" => "Iglesias Blázquez" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">1</span>" "identificador" => "aff1" ] ] ] 1 => array:3 [ "nombre" => "T." "apellidos" => "del Rosal Rabes" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "aff2" ] ] ] 2 => array:3 [ "nombre" => "E.P." "apellidos" => "Gutiérrez González" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "aff2" ] ] ] 3 => array:3 [ "nombre" => "J." "apellidos" => "Casas Rivero" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "aff2" ] ] ] 4 => array:3 [ "nombre" => "J.M." "apellidos" => "Marugán de Miguelsanz" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">1</span>" "identificador" => "aff1" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Servicio de Pediatría. Hospital de León. Madrid. España" "etiqueta" => "<span class="elsevierStyleSup">1</span>" "identificador" => "aff1" ] 1 => array:3 [ "entidad" => "Servicio de Pediatría. Hospital Universitario La Paz. Madrid. España" "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "aff2" ] ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "tieneResumen" => true "resumen" => array:1 [ "es" => array:1 [ "resumen" => "<span class="elsevierStyleSectionTitle">Objetivo</span><p class="elsevierStyleSimplePara elsevierViewall">Describir el síndrome linfedema-distiquiasis a raíz de la identificación de un caso clínico.</p> <span class="elsevierStyleSectionTitle">Material y métodos</span><p class="elsevierStyleSimplePara elsevierViewall">Se trata de una paciente de 13 años que acude por presentar un importante edema con fóvea en ambas piernas de 2 semanas de evolución sin otra sintomatología acompañante. En la exploración se detecta la presencia de doble línea de pestañas en párpados superiores e inferiores de ambos ojos (distiquiasis). La paciente fue ingresada para estudio realizándose múltiples exámenes complementarios (ecografía cardíaca y abdominal, Doppler de extremidades inferiores, función renal y hormonal), siendo el resultado de todos ellos normal. En el momento actual está pendiente de estudio genético para confirmar el diagnóstico de síndrome linfedema-distiquiasis. Se realizó búsqueda bibliográfica en PubMed con el objeto de encontrar información sobre casos clínicos similares.</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">1)</span> El síndrome linfedema-distiquiasis es un trastorno de herencia autosómica dominante íntimamente relacionado con mutaciones en el gen <span class="elsevierStyleItalic">FOXC2</span>, localizado en el cromosoma 16q. <span class="elsevierStyleItalic">2)</span> Es una rara entidad descrita en 1945 por Campbell caracterizada por distiquiasis desde el nacimiento y aparición de linfedema en miembros inferiores, generalmente en la segunda década de la vida y de curso crónico y recidivante. Se puede asociar a fisura palatina, defectos cardíacos y quistes extradurales. <span class="elsevierStyleItalic">3)</span> Se debe tener en cuenta la posibilidad de este síndrome en el diagnóstico diferencial de linfedema en adolescentes.</p>" ] ] ] "idiomaDefecto" => "es" "url" => "/16954033/0000006600000002/v2_201308271339/S1695403307703776/v2_201308271339/es/main.assets" "Apartado" => array:4 [ "identificador" => "14291" "tipo" => "SECCION" "es" => array:2 [ "titulo" => "Secciones de la A.E.P." "idiomaDefecto" => true ] "idiomaDefecto" => "es" ] "PDF" => "https://static.elsevier.es/multimedia/16954033/0000006600000002/v2_201308271339/S1695403307703776/v2_201308271339/es/main.pdf?idApp=UINPBA00005H&text.app=https://analesdepediatria.org/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403307703776?idApp=UINPBA00005H" ]
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