Esclerosis lateral amiotrofica pdf 2011

Amyotrophic lateral sclerosis is a chronic progressive neurodegenerative disease of unknown etiology. Office of communications and public liaison national institute of neurological disorders and stroke national institutes of health bethesda, md 20892. Esclerosis lateral amiotrofica genetic and rare diseases. Esclerosis lateral amiotrofica ela renut 2011 5 18. Orlando ruiz, our founder was diagnosed with als in march 2001. Green, gabriele ferlisi, giacomina ferrarese, valeria zullo, simona schirone, doretta oliva, a man with amyotrophic lateral sclerosis uses a mouth pressure microswitch to operate a text messaging system with a word prediction function, developmental neurorehabilitation, 20. It selectively affects both upper and lower motor neurons. Nowadays, amyotrophic lateral sclerosis is diagnosed on the basis of clinical and electromyographic findings and by ruling out other diseases with similar symptoms. Pr nigel leigh dr lokesh wijesekera ultima actualizacion. Amyotrophic lateral sclerosis matthew c kiernan, steve vucic, benjamin c cheah, martin r turner, andrew eisen, orla hardiman, james r burrell, margaret c zoing amyotrophic lateral sclerosis als is an idiopathic, fatal neurodegenerative disease of the human motor system. The disorder is named for its underlying pathophysiology, with amyotrophy referring to the atrophy of muscle fibers, which are denervated as their corresponding anterior horn cells degenerate.

Amyotrophic lateral sclerosis is a neurodegenerative disease with a survival rate up to 5 years of 20%. Riluzole is a benzothiazole derivative that modulates glutamatergic activity, thereby suppressing excitotoxicity. Esclerosis lateral amiotrofica linkedin slideshare. The colombian amyotrophic lateral sclerosis association acela is glad to be a new member of the international alliance of als mnd associations. The amyotrophic lateral sclerosis als is the most common form of motor neuron disease in the adulthood, and it is characterized by rapid and progressive compromise of the upper and lower motor. Hernando rafael 1, juan oscar david 2, antonio santiago vilca 1, jose luis aservi 1, maria del piar sanchez 1, andrey medvedyev 1, ronald viera 3, elcy mey lazo 1, haydee rivera 1, dasy elizabeth. Clinical diagnosis and management of amyotrophic lateral sclerosis, rev. Su causa es desconocida aunque hay varias hipotesis al respecto dano oxidativo, etc. Therapeutic trials in amyotrophic lateral sclerosis riluzole. Esclerosis lateral amiotrofica ela hoja informativaspanishlanguage fact sheet on. This drug modifies the course of als, but this treatment achieves only a modest improvement in survival 36 months. Amyotrophic lateral sclerosis als is the most common degenerative disease of the motor neuron system.