You can get it earlier though having it before 30 is very rare.
Als symptoms age range.
Although the disease can strike at any age symptoms most commonly develop between the ages of 55 and 75.
Als risk increases with age and is most common between the ages of 40 and the mid 60s.
Als is more commonly diagnosed in people between the ages of 40 to 70 although it s possible to be diagnosed at a younger age.
Although the mean survival time with als is three to five years some people live five 10 or more years.
Sixty percent of those suffering are men with a staggering 93 percent being caucasian.
Their median age at diagnosis was 67 years.
Most people get a diagnosis in their mid 50s.
About 5 10 of patients with als have the familial form.
Also women are less likely to develop als than men.
Average age at onset of amyotrophic lateral sclerosis als or lou gehrig s disease is 10 20 years old.
In most people with familial als their children have a 50 50 chance of developing the disease.
There are several potential risk factors for als including.
An als diagnosis usually happens between the ages of 40 and 60.
The average age at time of diagnosis is 55.
Answered on feb 8 2017 3 doctors agree.
Before the age of 65 slightly more men than women develop als.
Symptoms can begin in the muscles that control speech and swallowing or in the hands arms legs or feet.
They examined data covering 2 839 als patients diagnosed from 1995 through 2015 and classified them according to their disease symptoms as classic bulbar flail arm flail leg pumn and respiratory als.
Not all people with als experience the same symptoms or the same sequences or patterns of progression.
This sex difference disappears after age 70.
Amyotrophic lateral sclerosis does not present with gender specific symptoms but people with als report that a change in their voice or inability to grasp small objects was one of the first signs of the disorder explains the als association.
However as we age the difference between men and women disappears.
It s younger in patients with familial als than in patients with sporadic disease.