dc.creatorSan Martín Peñailillo, Pamela
dc.creatorSolís Flores, Fresia
dc.creatorCavada Chacón, Gabriel
dc.date.accessioned2019-03-18T12:03:53Z
dc.date.available2019-03-18T12:03:53Z
dc.date.created2019-03-18T12:03:53Z
dc.date.issued2018
dc.identifierRevista Chilena de Pediatria, Volumen 89, Issue 4, 2018, Pages 477-483
dc.identifier07176228
dc.identifier03704106
dc.identifier10.4067/S0370-41062018005000704
dc.identifierhttps://repositorio.uchile.cl/handle/2250/167700
dc.description.abstract© 2018, Sociedad Chilena de Pediatria. All rights reserved. Introduction: Duchenne muscular dystrophy (DMD) leads to a progressive deterioration of the muscle function and premature death. There are no longitudinal studies on the course of this pathology in Chile. Objective: To determine survival between the years 1993-2013, divided into two periods (1993-2002 and 2003-2013), and the effect of social determinants in patients with DMD admitted in Teleton Institutes of Chile (TI). Patients and Method:Prospective follow-up study in a clinical series of 462 patients with DMD. The information was obtained by searching for patients with DMD in OLAP cube (Online Analytical Processing). From the clinical records of the TI of Santiago, the variables corresponding to the diagnostic method, stage of DMD described in terms of muscle deterioration and function according to Swinyard classification were recorded; existence and type of tests that conclude the diagnosis and, in the cases reported, the
dc.languageen
dc.publisherSociedad Chilena de Pediatria
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceRevista Chilena de Pediatria
dc.subjectDuchenne muscular dystrophy
dc.subjectNeuromuscular disease
dc.subjectSurvival
dc.subjectSwinyard classification
dc.titleSurvival of patients with duchenne muscular dystrophy Sobrevida de pacientes con distrofia muscular de duchenne
dc.typeArtículos de revistas


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