Stiff-person syndrome
SPS is labeled as a rare disease. Stiff person syndrome SPS is a neurological disease with autoimmune features.
Stiff Person Syndrome Causes Symptoms Diagnosis Treatment
Stiff-person syndrome SPS is a rare acquired neurological disorder characterized by progressive muscle stiffness rigidity and repeated episodes of painful muscle spasms.
. Muscular rigidity often fluctuates ie grows worse and then improves and usually occurs along with the muscle spasms. Stiff person syndrome SPS is a rare progressive syndrome that affects the nervous system specifically the brain and spinal cord. Stiff person syndrome SPS is an autoimmune neurological disorder.
Stiff person syndrome SPS is a very rare disease affecting only one or two people per million. Autoimmune disorders including diabetes thyroiditis vitiligo and pernicious anemia. Stiff person syndrome is more likely seen in people with certain types of diseases including.
An autoimmune and neurological disorder that causes rigidity and spasms in the trunk and limbs. Spasms can generate enough force to fracture bone. Muscle rigidity sporadic muscle spasms and chronic muscle pain characterize SPS.
Stiff-person syndrome SPS is a rare and disabling central nervous system disorder with no satisfactory treatment. Stiff-person syndrome SPS is a rare neurological disorder with features of an autoimmune disease. A small minority of patients have.
It causes progressive muscle stiffness and painful spasms that can be triggered by a variety of things including sudden movement cold temperature or unexpected loud noises. Why Choose Johns Hopkins. Stiff-person syndrome also known as stiff-man syndrome is a rare neurologic disorder of unclear cause characterized by progressive rigidity and stiffness.
Certain cancers including breast lung kidney thyroid colon and Hodgkins lymphoma. SPS is characterized by fluctuating muscle rigidity in the trunk and limbs and a heightened sensitivity to stimuli such as noise touch and emotional distress which can set off muscle spasms. Chronic pain impaired mobility and lumbar hyperlordosis are common symptoms.
Medications and immunotherapy maybe prescribed with aqua occupational and physical therapy. The stiffness primarily affects the truncal muscles and is superimposed by spasms resulting in postural deformities. But more people are affected than reported due to misdiagnoses.
SPS occurs in about one in a million people and is most commonly found in middle-aged people. Symptoms may include extreme muscle stiffness rigidity and painful spasms in the trunk and limbs severely impairing mobility. Muscle spasms can be so violent they can dislocate joints and even break bones.
Symptoms include stiffening in the torso and limbs along with episodes of severe muscle spasms. Like other types of neurological disorders SPS affects your brain and spinal cord central nervous system. SPS is strongly correlated with autoimmune diseases and it is usual to find high titers of antibodies against acid decarboxylase GAD65.
Symptoms include muscle spasms hyper-rigidity debilitating pain and chronic anxiety.
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