Myopathy is a neuromuscular disorder that impairs skeletal muscle function without affecting the nervous system. It can be caused by inherited genetic disorders, infections, or acquired conditions like muscle fatigue. The main symptoms are muscle weakness, inflammation, spasms, and paralysis. Those susceptible include people with a genetic predisposition who develop symptoms in childhood or early adulthood. The disease affects muscle relaxation and can cause stiffness, especially after periods of rest or cold exposure. Treatment focuses on avoiding triggers and potentially using medications to reduce symptoms.
Myopathy is a neuromuscular disorder that impairs skeletal muscle function without affecting the nervous system. It can be caused by inherited genetic disorders, infections, or acquired conditions like muscle fatigue. The main symptoms are muscle weakness, inflammation, spasms, and paralysis. Those susceptible include people with a genetic predisposition who develop symptoms in childhood or early adulthood. The disease affects muscle relaxation and can cause stiffness, especially after periods of rest or cold exposure. Treatment focuses on avoiding triggers and potentially using medications to reduce symptoms.
Myopathy is a neuromuscular disorder that impairs skeletal muscle function without affecting the nervous system. It can be caused by inherited genetic disorders, infections, or acquired conditions like muscle fatigue. The main symptoms are muscle weakness, inflammation, spasms, and paralysis. Those susceptible include people with a genetic predisposition who develop symptoms in childhood or early adulthood. The disease affects muscle relaxation and can cause stiffness, especially after periods of rest or cold exposure. Treatment focuses on avoiding triggers and potentially using medications to reduce symptoms.
inflammation, tetany (spasms), or paralysis. Myopathy can be the result of either inherited or acquired causes.
Others are linked to exposure to an infectious agent,
such as viruses or bacteria, or are inherited.
Myopathy develops as the result of either inherited
(congenital or genetic) disorders or acquired conditions of the muscles. Most commonly, people develop acquired myopathy from muscle fatigue, electrolyte imbalance, or dehydration, resulting in stiffness or cramping. Other causes of myopathy
How does myopathy affects the
muscular system?
Central core disease: mild weakness of voluntary muscles,
especially in the hips and legs; hip displacement; delays in reaching developmental motor milestones; problems with running, jumping, and climbing stairs develop in childhood
Centro nuclear myopathy: weakness of voluntary muscles including
those on the face, arms, legs, and trunk; drooping upper eyelids; facial weakness; foot drop; affected muscles almost always lack reflexes
Myotonic congenital: voluntary muscles of the arms, legs, and face
are stiff or slow to relax after contracting (myotonic); stiffness triggered byfatigue, stress, cold, or long rest periods, such as a night's sleep; stiffness can be relieved by repeated movement of the affected muscles
Who is more susceptible to get
myopathy? Genes
are responsible for building our bodies;
we inherit them from our parents along with any mutations or defects they have and pass them on to our children.
Early
to late childhood
Signs and symptoms
The
main problems faced by people with this
disease are delayed muscle relaxation and muscle stiffness. Typically provoked by sudden movements after rest.
Cold
exposure can have similar effects, but
some people experience muscle stiffness, weakness or, sometimes, temporary paralysis even when theyre warm.
Treatment
By
avoiding strenuous exercise and cold, most
people with this condition can largely escape disability. But medications can be beneficial, especially for those who experience symptoms independent of exercise and cold. Your MDA clinic director can give you more information about these medications.