As of the latest data, there are approximately 5,000 people living with amyotrophic lateral sclerosis (ALS) in the UK. The incidence of ALS is about 1-2 cases per 100,000 people annually. While the exact numbers can fluctuate, ALS remains a relatively rare neurological condition compared to other diseases. For the most accurate and current statistics, it's advisable to consult health organizations or research studies focused on ALS in Britain.
Approximately 5,600 people in the U.S. are diagnosed with ALS each year. There are approximately 30,000 cases of ALS in the U.S. at any given time. the real question is how do you get it or how can u get it
Brittian Scott is 5' 9".
Amyotrophic lateral sclerosis (ALS) can be hereditary in some cases, known as familial ALS, which accounts for about 5-10% of all cases. The majority of ALS cases are sporadic, meaning they occur without a clear genetic link. Certain genetic mutations, such as those in the C9orf72, SOD1, and TARDBP genes, have been associated with familial ALS. However, even in sporadic cases, genetic factors may still play a role alongside environmental influences.
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ALS usually progresses rapidly, and leads to death from respiratory infection within three to five years in most cases.
There is no way to tell, but in most cases of als its men between ages 30 and older. Hope it helped.
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ALS progresses rapidly in most cases. It is fatal within three years for 50% of all people affected, and within five years for 80%. Ten percent of people with ALS live beyond eight years.
In ALS, also known as amyotrophic lateral sclerosis, the chromosome primarily affected is chromosome 9. A gene called C9orf72 located on this chromosome is linked to a significant percentage of familial ALS cases. Other genetic mutations on different chromosomes can also contribute to ALS development.
Great Brittian
Journalist, teacher and a nurse!