Esclerosis lateral amiotrofica by mariela moron on prezi. Early care and palliative support in als lead to an improvement in survival and. Amyotrophic lateral sclerosis is a neurodegenerative disease with devastating consequences for the patient and hisher family. Amyotrophic lateral sclerosis als, charcots disease or lou gehrigs disease, is a term used to cover the spetrum of syndromes caracterized by progressive degeneration of motor neurons, a paralytic disorder caused by motor neuron degeneration. Sobrevida en pacientes con esclerosis lateral amiotrofica redalyc. In the last 20 years, over 25 als genes were discovered. Issuu is a digital publishing platform that makes it simple to publish magazines, catalogs, newspapers, books, and more online. Amyotrophic lateral sclerosis als is a neurodegenerative disease of unknown etiology characterized by death of motor neurons. Presently, als is considered a complexed multifactorial disorder of unknown etiology. Amyotrophic lateral sclerosis als is a progressive neurodegenerative adult onset disease. Abstract the amyotrophic lateral sclerosis, is historically an important illness inside the neurodegeneration diseases, by the different demonstrations that involve so much signs of lower and upper motor neuron. Easily share your publications and get them in front of issuus.
Esclerosis lateral amiotrofica, fisiopatologia, cuadro clinico, diagnostico, tratamiento. Actividad fisica y salud milvar pedro santos contreras. Sobrevida en pacientes con esclerosis lateral amiotrofica serra. Jean martin charcot 1869 introduccion famosos con esta enfermedad.
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