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In addition, the patient mentions lesser profuse symptoms in his first-degree relative (father). These two major criteria allow us to diagnose the symptoms as neurofibromatosis type 1.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span>" "pdfFichero" => "main.pdf" "tienePdf" => true "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Domínguez-Enríquez J, Cueva-Rosillo J, Cusco-Cuzco C, Cuzco-Naranjo X, Diagnóstico rápido, neurofibromatosis tipo 1. 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Journal Information
Vol. 146. Issue 4.
Pages e23 (February 2016)
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Vol. 146. Issue 4.
Pages e23 (February 2016)
Image in medicine
Fast diagnosis of type 1 neurofibromatosis
Diagnóstico rápido, neurofibromatosis tipo 1
Juan Domínguez-Enríqueza,
, Juana Cueva-Rosillob, Cristian Cusco-Cuzcoc, Ximena Cuzco-Naranjod
Corresponding author
a Centro de Biomedicina, Carrera de Medicina, Universidad Central del Ecuador, Quito, Ecuador
b Departamento de Emergencia, Hospital Carlos Andrade Marín, Quito, Ecuador
c Departamento de Emergencia, Hospital Enrique Garcés, Quito, Ecuador
d Departamento de Medicina Interna, Hospital de las Fuerzas Armadas, Quito, Ecuador
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