Analysis and design of a passive assistive device for patients with Duchenne Muscular Dystrophy
Visualitza/Obre
Estadístiques de LA Referencia / Recolecta
Inclou dades d'ús des de 2022
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hdl:2117/361641
Tipus de documentText en actes de congrés
Data publicació2021
Condicions d'accésAccés obert
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Reconeixement-NoComercial-SenseObraDerivada 3.0 Espanya
Abstract
Duchenne Muscular Dystrophy (DMD) is the most common muscular dystrophy diagnosed during childhood and is characterized by progressive muscle weakness and loss of muscle mass. DMD is a genetic disease that causes alterations in the dystrophin protein, which protects muscle fibers. Without dystrophin, muscles are broken down by enzymes, which leads to the death of muscle cells and tissue, and causes degeneration and muscle weakness. Because DMD is inherited in an X-linked recessive pattern, it manifests mainly in males (1 in 5000). The mutation of the gene is usually transmitted from mother to child, but it may also occur by spontaneous mutations
CitacióComas, P. [et al.]. Analysis and design of a passive assistive device for patients with Duchenne Muscular Dystrophy. A: Reunión del Capítulo Español de la Sociedad Europea de Biomecánica. "Libro de Resúmenes de la X Reunión del Capítulo Español de la Sociedad Europea de Biomecánica". 2021, p. 76-77. ISBN 978-84-338-6931-9.
ISBN978-84-338-6931-9
Altres identificadorshttps://drive.google.com/file/d/1m4lvL0yplCiSbqIjBhyZXWRaFZzzaaKc/view
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