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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Presentamos un caso de s&#237;ndrome de EhIers-Danlos en su forma cl&#225;sica que debido a la hiperlaxitud articular y ligamentosa se acompa&#241;a de complicaciones ortop&#233;dicas y deformidades esquel&#233;ticas de diverso tipo&#46; Pectus carinatum con escoliosis secundaria pocas veces descrito&#44; displasia de cadera&#44; genu recurvatum&#44; pie plano valgo&#46; Adem&#225;s presentaba osteoprosis generalizada y dedos supernumerarios que no hemos encontrado escritos en la literatura&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Entre los antecedentes familiares se han encontrado alteraciones tor&#225;cicas del mismo tipo que no hemos podido estudiar&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Por &#250;ltimo&#44; la indicaci&#243;n quir&#250;rgica ha sido hecha desde el punto de vista est&#233;tico a pesar de no presentar ninguna sintomatolog&#237;a cardiorespiratoria seg&#250;n la t&#233;cnica de Ravit&#46;</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Los resultados inmediatos han sido satisfactorios &#40;fig&#46; 9&#41; habi&#233;ndose reducido la deformidad&#44; sin embargo&#44; la cicatriz a pesar del injerto es anfractuosa&#44; atr&#243;fica&#44; como ocurre habitualmente en este s&#237;ndrome&#46;</p></span>"
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        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">The authors present a case of Ehlers-Danlos&#8217; syndrome in its classical form that due to articular and ligamentous hyperlaxity was accompanied by orthopedic complications and skeletal deformities of various types&#44; pectus carinatum with secondary scoliosis seldom described&#44; dysplasia of the hip&#44; genu recurvatum&#44; pes planovalgus&#46; There was also generalized osteoporosis and supernumerary fingers that the authors have not found described in medical literature&#46;</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">In the familial antecedents there were thoracic alterarions of the same type&#44; but they could not be studied&#46;</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Finally&#44; the surgical indication was made from the esthetic point of view in spite of not presenting any cardiorespiratory symptomatology according to Ravit&#39;s technique&#46;</p><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">The immediate results have been satisfactory&#46; The deformity was reduced&#44; how ever&#44; in spite of the graft&#44; the scar in anfractuous&#44; astrophic as habitually&#46; occurs in this syndrome&#46;</p></span>"
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Sindrome de ehlers-danlos asociado a pectus carinatus
Ehlers danlos’ syndrome associated with pectus carinatum
J.M. Rodríguez Paniagua, J.A. Pérez Antón, J.L. Martín de Nicolás, Serrahima, J. Toledo González, M. Palazón de la Barreda
Sección de Cirugía Torácica. Ciudad Sanitaria de la S.S. «Io de Octubre», Madrid
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        "titulo" => "Resumen"
        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Presentamos un caso de s&#237;ndrome de EhIers-Danlos en su forma cl&#225;sica que debido a la hiperlaxitud articular y ligamentosa se acompa&#241;a de complicaciones ortop&#233;dicas y deformidades esquel&#233;ticas de diverso tipo&#46; Pectus carinatum con escoliosis secundaria pocas veces descrito&#44; displasia de cadera&#44; genu recurvatum&#44; pie plano valgo&#46; Adem&#225;s presentaba osteoprosis generalizada y dedos supernumerarios que no hemos encontrado escritos en la literatura&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Entre los antecedentes familiares se han encontrado alteraciones tor&#225;cicas del mismo tipo que no hemos podido estudiar&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Por &#250;ltimo&#44; la indicaci&#243;n quir&#250;rgica ha sido hecha desde el punto de vista est&#233;tico a pesar de no presentar ninguna sintomatolog&#237;a cardiorespiratoria seg&#250;n la t&#233;cnica de Ravit&#46;</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Los resultados inmediatos han sido satisfactorios &#40;fig&#46; 9&#41; habi&#233;ndose reducido la deformidad&#44; sin embargo&#44; la cicatriz a pesar del injerto es anfractuosa&#44; atr&#243;fica&#44; como ocurre habitualmente en este s&#237;ndrome&#46;</p></span>"
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        "titulo" => "Summary"
        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">The authors present a case of Ehlers-Danlos&#8217; syndrome in its classical form that due to articular and ligamentous hyperlaxity was accompanied by orthopedic complications and skeletal deformities of various types&#44; pectus carinatum with secondary scoliosis seldom described&#44; dysplasia of the hip&#44; genu recurvatum&#44; pes planovalgus&#46; There was also generalized osteoporosis and supernumerary fingers that the authors have not found described in medical literature&#46;</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">In the familial antecedents there were thoracic alterarions of the same type&#44; but they could not be studied&#46;</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Finally&#44; the surgical indication was made from the esthetic point of view in spite of not presenting any cardiorespiratory symptomatology according to Ravit&#39;s technique&#46;</p><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">The immediate results have been satisfactory&#46; The deformity was reduced&#44; how ever&#44; in spite of the graft&#44; the scar in anfractuous&#44; astrophic as habitually&#46; occurs in this syndrome&#46;</p></span>"
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Article information
ISSN: 03002896
Original language: Spanish
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