Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) is a progressive nervous system disorder. It gradually destroys the nerves responsible for muscle movement. Over time, ALS ...
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Definition
Amyotrophic lateral sclerosis (ALS) is a progressive nervous system disorder. It gradually destroys the nerves responsible for muscle movement. Over time, ALS leads to almost total paralysis of muscle movement, including respiration.
Prognosis is poor in most cases because of the progressive nature of the condition and the eventual respiratory failure. After diagnosis is made, life span ranges from 2-5 years. The five-year survival rate ranges from 14%-25%, and up to 10% of patients will survive more than 10 years. In general, the younger the age of onset, the slower the disease progresses.
The Nervous System
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Causes
The cause of ALS is not known, but in a small number of cases, it appears that genes may have played a role. Also, research has shown that there may be a reduced response to cell stress, as well as cell toxicity, related to certain protein build-up in the brain.
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Risk
A risk factor is something that increases your chance of getting a disease or condition. Risk factors include:
- Having a family member with ALS
- Being in the military or having other occupations
- Having certain genetic mutations
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Symptoms
Symptoms include:
- Progressive weakness in arms and legs (at first often on only one side) over weeks to months without changes in sensory abilities.
- Initial presentation may be a wrist or foot drop
- Trouble holding things without dropping them
- Frequent tripping while walking
- Shrunken muscles
- Twitchy muscles
- Unpredictable changing emotions
- Clumsiness
- Overactive reflexes
- Slurred speech
- Hoarseness
- Trouble chewing and swallowing, resulting in frequent choking and gagging
- Weight loss due to trouble eating
- Trouble breathing
- Excess salivation, drooling
- Cognition is intact
- Sensation is intact
- Trouble coughing, resulting in development of pneumonia
- diagnosis
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Diagnosis
The doctor will ask about your symptoms and medical history, and do a physical exam. There are no tests that definitively diagnose ALS, but tests may be used to rule out other medical conditions.
Tests may include:
- Electromyogram (EMG) —to look for progressive muscle weakness and twitching
- CT Scan —a type of x-ray that uses a computer to make pictures of the structures inside the head and spine
- MRI Scan —a test that uses magnetic waves to make pictures of the structures inside the head and spine
- Blood tests—to rule out metabolic, heavy metal exposure, or rarely infections (eg, Lyme disease, HIV, human T-lymphotropic virus)
- Lumbar puncture —a procedure to collect cerebrospinal fluid (CSF)
- Urine tests
- treatment
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Treatment
There is currently no cure for ALS.
For you and your family, a multidisciplinary approach may work best. This approach may include:
- Taking medicines
- Working with therapists and joining a support group
- Participating in religious and social activities
Treatments options include:
MedicationsThe drug riluzole has been approved for ALS with a clinical trial revealing a modest lengthening of survival. The drug may slightly improve functioning, but it does not stop the disease from progressing. Other drugs are also being studied.
Your doctor may prescribe these medicines for symptoms
- Diazepam (eg, Valium), baclofen (eg, Lioresal), or dantrolene —to reduce spasticity
- Nonsteroidal anti-inflammatory drugs (NSAIDs) and other pain medicines
- Atropine (eg, AtroPen), scopolamine (eg, Isopto), botulinum toxin (eg, Botox), antihistamine—to reduce heavy drooling
- Antidepressants and anti-anxiety medicines
- A combination of dextromethorphan and quinidine —to treat inappropriate laughter or crying
Other Types of Treatments- Physical therapy—This is used to reduce pain associated with muscle cramping and spasticity.
- Respiratory care—In some cases, you may need to receive a mixture of air and oxygen from a machine. If you cannot move enough air in and out of your lungs, you may need surgery to have a tube inserted into your airway.
- Nutritional care—Your doctor may make changes to your diet. In some cases, getting nutrition through tube feeding is needed.
- Speech therapy—Speech therapy may be used to optimize communication. Therapy can include exploring alternative methods of communication.
- prevention
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Prevention
There are no guidelines for preventing ALS because the cause is unknown.
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