Amyotrophic Lateral Sclerosis | Spain| PDF | PPT| Case Reports | Symptoms | Treatment

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis

    Amyotrophic horizontal sclerosis or ALS, is a sensory system (neurological) sickness that causes muscle shortcoming and effects physical capacity. The characterizing highlight of ALS is the demise of both upper and lower engine neurons in the engine cortex of the cerebrum, the mind stem, and the spinal string. Before their pulverization, engine neurons create protein-rich incorporations in their cell bodies and axons. This may be somewhat because of imperfections in protein degradationThese considerations regularly contain ubiquitin, and by and large consolidate one of the ALS-related proteins: SOD1, TAR DNA tying protein.

  • Amyotrophic Lateral Sclerosis

    Symptoms: The onset of ALS may be so subtle that the symptoms are overlooked. The earliest symptoms may include fasciculations, cramps, tight and stiff muscles (spasticity), muscle weakness affecting an arm or a leg, slurred and nasal speech, or difficulty chewing or swallowing.

  • Amyotrophic Lateral Sclerosis
    ALS is a fatal disease with no effective treatment and no cure. Eighty per cent of people with ALS die within two to five years of diagnosis. Some people die within a few months. Ten per cent of those affected may live 10 years or longer. ALS is the most common cause of neurological death. The mortality rate for ALS is approximately 2/100,000 per year and approximately 2,500 - 3,000 people over 18 currently live with
Expert PPTs
Speaker PPTs

High Impact List of Articles

Conference Proceedings