An introduction to the issue of amyotrophic lateral sclerosis als

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An introduction to the issue of amyotrophic lateral sclerosis als

Amyotrophic lateral sclerosis ALS is a degenerative disease that affects the brain and spinal cord. ALS is a chronic disorder that causes a loss of control of voluntary muscles.

The nerves controlling speech, swallowing, and limb movements are often affected.

Introduction to Amyotrophic Lateral Sclerosis (ALS) | Causes of ALS |

Unfortunately, a cure has not yet been found for it. The famous baseball player Lou Gehrig was diagnosed with the disease in ALS can be classified as either sporadic or familial. Most cases are sporadic. That means no specific cause is known. Some factors that scientists think might contribute to ALS include: The onset of symptoms in ALS usually occurs between the ages of 50 and 60, although symptoms can occur earlier.

ALS is slightly more common in men than in women. They also estimate that around 20, Americans are currently living with the disorder.

ALS affects people in all racial, social, and economic groups. This condition is also becoming more common. This may be because the population is aging. Both sporadic and familial ALS are associated with a progressive loss of motor neurons. The symptoms of ALS depend on what areas of the nervous system are affected.


These will vary from person-to-person. The medulla is the lower half of the brainstem. These include breathing, blood pressure, and heart rate.

An introduction to the issue of amyotrophic lateral sclerosis als

Damage to the medulla can cause:Being diagnosed with Amyotrophic Lateral Sclerosis (ALS) can be Cord Injury · Traumatic Brain Injury · Enhanced muscle activity · Better range of motionProgram: Apply Now, Lokomat Advantage, Muscle Memory and more.

Introduction. Amyotrophic lateral sclerosis (ALS) is a devastating and almost universally fatal neurodegenerative disease. Very rarely, a person who is diagnosed with ALS stops progressing and regains significant motor function. Amyotrophic lateral sclerosis (ALS) is a relatively rare disease with a reported population incidence of between and per per year.

Over the past 10 years, the design of ALS epidemiological studies has evolved to focus on a prospective, population based methodology, employing the El Escorial criteria and multiple sources of data to ensure complete case ascertainment. Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND), or Lou Gehrig's disease, is a specific disease which causes the death of neurons controlling voluntary muscles.

A comprehensive review of amyotrophic lateral sclerosis

Some also use the term motor neuron disease for a group of conditions of which ALS is the most common. Next article in issue; Introduction. Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder of upper and lower motor neurons that causes progressive paralysis and eventually death from respiratory failure.

1 The course of ALS varies substantially between people. In a small phase 1 trial, investigators found that the infusion of autologous regulatory T-lymphocytes in ALS patients correlated with slower disease progression.


The idea that neuroinflammation could be a key player in amyotrophic lateral sclerosis (ALS) has generated research in animal models of the disease for almost two decades.

Amyotrophic lateral sclerosis - Wikipedia