Amiortrophic lateral sclerosis

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Nutritionists can advise on preparing nutritious meals that are easier to swallow. Myasthenic syndromealso known as Lambert—Eaton syndrome, can mimic ALS, and its initial presentation can be similar to that of myasthenia gravis MGa treatable autoimmune disease sometimes mistaken for ALS.

Marked weight loss occurs in approximately 5 percent of cases. Flail arm syndrome and flail leg syndrome are often considered to be regional variants of PMA because they only involve lower motor neurons. Clinical trials Many neurological disorders do not have effective treatment options.

The risk of transmitting the disease to the children of a couple, both of whom are carriers for a recessive disorder, is 25 percent.

Chromosomes are found in the nucleus of all body cells. However, some people with ALS live 10 or more years.

als life expectancy
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Amyotrophic Lateral Sclerosis