dc.contributorMateus Arbelaez, Heidi Eliana
dc.creatorEslava Otálora, Andrea Cecilia
dc.date.accessioned2016-08-31T13:26:24Z
dc.date.available2016-08-31T13:26:24Z
dc.date.created2016-08-31T13:26:24Z
dc.date.issued2016
dc.identifierhttp://repository.urosario.edu.co/handle/10336/12351
dc.identifierhttps://doi.org/10.48713/10336_12351
dc.description.abstractINTRODUCTION. Duchenne muscular dystrophy is a neuromuscular disease with X-linked recessive inheritance that affects 1 in 3, 500 live births. It is caused by mutations in the DMD gene coding for dystrophin. It is characterized by typical variable clinical manifestations of progressive proximal muscular dystrophy. OBJECTIVE. Perform the first registry in Colombia of patients identified with dystrophinopathies, taking into account clinical and paraclinical characteristics and causal mutations of this disease. METHODOLOGY It is a transversal, descriptive study of the review of medical records of patients diagnosed with DMD treated at the Genetics unit at the University of Rosario during the years 2006-2015. RESULTS 99 patients were identified, of which 56 (56. 56%) correspond to Duchenne phenotype and 12 (12. 12%) to Becker. It was not possible to classify 31 patients (31. 3%) due to lack of clinical data. The age of onset of symptoms was on average 4. 41 years. The most frequent mutations were deletions (69%), followed by point mutations (14%), duplication (11%) and other mutations (4%). CONCLUSIONS This registry of dystrophinopathies is the first reported in Colombia and the starting point to determine the incidence of the disease, clinical and molecular characterization of patients, ensuring timely access to new medical treatments precision to improve the quality of life of patients and their families
dc.languagespa
dc.publisherUniversidad del Rosario
dc.publisherMaestría en Ciencias con Énfasis en Genética Humana
dc.publisherFacultad de medicina
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto completo)
dc.rightsEL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma. PARGRAFO: En caso de presentarse cualquier reclamación o acción por parte de un tercero en cuanto a los derechos de autor sobre la obra en cuestión, EL AUTOR, asumirá toda la responsabilidad, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos la universidad actúa como un tercero de buena fe. EL AUTOR, autoriza a LA UNIVERSIDAD DEL ROSARIO, para que en los términos establecidos en la Ley 23 de 1982, Ley 44 de 1993, Decisión andina 351 de 1993, Decreto 460 de 1995 y demás normas generales sobre la materia, utilice y use la obra objeto de la presente autorización. -------------------------------------- POLITICA DE TRATAMIENTO DE DATOS PERSONALES. Declaro que autorizo previa y de forma informada el tratamiento de mis datos personales por parte de LA UNIVERSIDAD DEL ROSARIO para fines académicos y en aplicación de convenios con terceros o servicios conexos con actividades propias de la academia, con estricto cumplimiento de los principios de ley. Para el correcto ejercicio de mi derecho de habeas data cuento con la cuenta de correo habeasdata@urosario.edu.co, donde previa identificación podré solicitar la consulta, corrección y supresión de mis datos.
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dc.sourceinstname:Universidad del Rosario
dc.sourcereponame:Repositorio Institucional EdocUR
dc.subjectDistrofia muscular de Duchenne
dc.subjectDistrofia muscular de Becker
dc.subjectDistrofinopatías
dc.titleRegistro de pacientes con distrofinopatías en Colombia
dc.typemasterThesis


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