Verified By Apollo Hospitals October 1, 2024
Primary lateral sclerosis or PLS is a disease where the nerve cells in the brain that control movement, which is also called upper motor neurons, slowly break down and fail over time.
This prevents the nerves from activating the motor neurons present within the spinal cord controlling the muscles. Primary lateral sclerosis or PLS results in weakening of the voluntary muscles that are used to control the arms, tongue and legs.
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When the central nerve cells are unable to activate the motor neurons in the spinal cord, which control voluntary muscles, it can cause movement problems like slowed movement and clumsiness, difficulty with balance, weakness and problems with swallowing and speech.
Primary lateral sclerosis is also known as progressive upper motor neuron dysfunction, in the absence of the clinical symbols of the lower motor neuron participation or family history suggestive of hereditary spastic paraplegia.
Primary lateral sclerosis is one of the sporadic motor neuron disorders, comprising progressive muscular atrophy (only lower motor neuron) and amyotrophic lateral sclerosis (mixed lower and upper motor neuron participation). It is a rare disorder with two types , one affecting adults and a juvenile form .
The signs and symptoms of primary lateral sclerosis are:
Signs and symptoms of primary lateral sclerosis generally take years to progress and usually begin in the legs.
Less frequently, primary lateral sclerosis starts in the hands and the tongue and after some time, it reaches the spinal cord and then the legs.
Consult your doctor if you are facing complications like stiffness or weakness in the legs or while speaking and swallowing. If your child is growing and facing spasticity in the voluntary muscles or is losing balance abnormally, then make an appointment with a pediatrician.
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In PLS, the nerve cells that are present in the brain start failing with the passage of time. This loss results in movement complications, like slow movements, issues in balancing and bungling. The major cause of adult PLS is still not discovered. In the maximum number of cases, it is not a genetic disease.
Mutations in a gene called ALS2 causes juvenile PLS (primary lateral sclerosis). ALS2 gene gives instructions to create a protein called alsin, which is present in motor neuron cells. If alsin becomes unstable, it may in turn, impair normal muscle function. Juvenile PLS is an autosomal recessive inherited disease, which means that both the parents have to be the carriers of the gene to pass it on to their child, even though they themselves do not have the disease.
There is no treatment to prevent or stop primary lateral sclerosis. However, the treatment which focuses on providing relief from the symptoms and preserving functions consists of:
-Medications like baclofen, clonazepam, tizanidine, etc. to relieve the stiffness. You have to take these medications orally.
– If you are not able to control the stiffness issue with the oral medication, your doctor would’ve to perform a surgery for inserting a medication pump to supply baclofen to your spinal fluid.
-Some antidepressants may be presecribed if you are suffering from the problem.
-Physical therapy too helps in treating this disorder while stretching activities or exercises help in maintaining the strength of the muscle and providing uninterrupted mobility to the joints. Heating pads also relieve muscle pain.
-If the facial muscles are affected due to PLS, speech therapy is also an option to get relief.
– Physical therapists can also suggest some assistive devices like a cane, wheelchair, walker, etc.
Primary lateral sclerosis is not fatal in nature. However, there is no possible cure and the progression of the indications varies. Some people can preserve the ability to walk without any support or assistance, but others will ultimately need wheelchairs, walkers, canes, etc.
It is more common in men with a gradual onset between the ages of 40 and 60. Primary lateral sclerosis develops progressively over a number of years or sometimes even decades.
Unlike amyotrophic lateral sclerosis (ALS), the prognosis in primary lateral sclerosis is slower . However, primary lateral sclerosis is a progressive disorder.
This disorder commonly starts in the legs but can begin in the upper body muscles as well.
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