- Amyotrophic Lateral Sclerosis (ALS)
- What is the difference between ALS and MS (Multiple Sclerosis)?
- What are the different types of MND (motor neuron disease)?
- What are the symptoms of ALS?
- What are the causes of ALS?
- What are the risk factors and complications of ALS?
- How is ALS diagnosed?
- What is the treatment for ALS?
- Coping with ALS and outlook
What are the different types of MND (motor neuron disease)?
There are four different types of MND, each one of them has different effects, however, they can also overlap each other in a number of ways.
The following is a brief outline of the four main types of MND:
Amyotrophic Lateral Sclerosis (ALS)
This is known as the most common type of MND and is the focus of this article. This condition involves both the lower and upper neurons in the central nervous system. The characteristics of this condition are defined by the wasting and weakness of the limbs due to nerve cell deterioration (i.e. neurodegeneration). The average life expectancy is between two and five years from the onset of the initial symptoms.
Upper motor neurons originate in the cerebral cortex or in the brain stem and transport motor information to the lower motor neurons. The lower motor neurons stem from the spinal cord to specific muscles.
Progressive Bulbar Palsy (PBP)
This condition affects both the lower and upper motor neurons. The symptoms are often those of slurred speech and difficulty in swallowing. The life expectancy of a sufferer is between six months to three years from the onset of the initial symptoms.
Progressive Muscular Atrophy (PMA)
The condition only affects a small amount of people and mainly results in damage to the lower motor neurons. The early symptoms are often seen in the affected person acting exceptionally clumsy or experiencing weakness in their hands. The life expectancy for those with this condition is normally more than five years.
Primary Lateral Sclerosis (PLS)
This is a very rare type of MND and only involves the upper motor neurons. The condition results in a weakness in one’s lower limbs and some people also suffer from weakness in their hands and speech issues. The sufferer’s lifespan is typically normal, however, this condition can also develop into ALS which will affect the outcome significantly.
What are the two types of ALS?
ALS can either be classified as familial ALS or sporadic ALS. These are explained as follows:
- Familial ALS (fALS) – This type of ALS runs in families and is very rare. Roughly 5-10% of patients have familial ALS, meaning they have inherited it from their parent due to a gene mutation in their DNA.
- Sporadic ALS – This is ALS that is not inherited and roughly 90% of patients have this kind, meaning they are the only one in their family with the disease. The exact cause is not yet understood, however, researchers believe that it may be a combination of genetic and environmental risks.