Sclerosis, amyotrophic lateral treatment in hyderabad

overview

symptom

The signs and symptoms of ALS vary widely from person to person, depending on the neurons affected. Signs and symptoms can include:

The reasons

ALS affects the nerve cells that control voluntary muscle movements such as walking and speaking (motor neurons). ALS causes the progressive deterioration of motor neurons, followed by their death. Motor neurons extend from the brain to the spinal cord to muscles throughout the body. When the motor neurons are damaged, they stop sending messages to the muscles, causing the muscles to stop working. Sclerosis, amyotrophic lateral treatment in Nizamabad

ALS is inherited by 5% to 10% of people. Otherwise the cause is unknown.

Risk factors

Established risk factors for ALS include:

Inheritance. Five to 10 percent of people with ALS have inherited it (familial ALS). For most people with familial ALS, their children have a 50-50 chance of developing the disease.
Age. The risk of ALS increases with age and is more common between the ages of 40 and the mid-60s.
Sex. Before the age of 65, slightly more men than women develop ALS. This gender difference disappears after 70 years.

Complications

In the course of the disease, ALS leads to complications such as:

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