Stiff person syndrome

Stiff person syndrome SPS is a rare autoimmune neurological disorder. Stiff Person Syndrome SPS is an autoimmune and neurological disorder that can make the muscles in the torso and limbs alternate between rigidity and spasms.


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Serum anti-GAD glutamic acid decarboxylase 65 antibody serum amphiphysin antibody several other serum autoantibodies hemoglobin A1c and vitamin levels lumbar puncture MRI of the brain and spine neurophysiological studies.

. But more people are affected than reported due to misdiagnoses. The cause of this extremely rare disease is still unknown. Stiff-person syndrome SPS is a rare and disabling central nervous system disorder with no satisfactory treatment.

The stiffness primarily affects the truncal muscles and is superimposed by spasms resulting in postural deformities. Muscle rigidity sporadic muscle spasms and chronic muscle pain characterize SPS. 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 a rare neurological disorder with features of an autoimmune disease. SPS occurs in about one in a million people and is most commonly found in middle-aged people. SPS is strongly correlated with autoimmune diseases and it is usual to find high titers of antibodies against acid decarboxylase GAD65.

Tests for diagnosing stiff person syndrome may include the following. Spasms can generate enough force to fracture bone. A small minority of patients have.

Stiff person syndrome SPS is a neurological disease with autoimmune features. Chronic pain impaired mobility and lumbar hyperlordosis are common symptoms. Stiff person syndrome is more likely seen in people with certain types of diseases including.

Stiff-person syndrome also known as stiff-man syndrome is a rare neurologic disorder of unclear cause characterized by progressive rigidity and stiffness. Autoimmune disorders including diabetes thyroiditis vitiligo and pernicious anemia. Stiff-person syndrome SPS is a rare acquired neurological disorder characterized by progressive muscle stiffness rigidity and repeated episodes of painful muscle spasms.

Learn more about the treatment and outlook for the condition here. 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. Abnormal postures often hunched.

Muscular rigidity often fluctuates ie grows worse and then improves and usually occurs along with the muscle spasms. SPS is labeled as a rare disease. Certain cancers including breast lung kidney thyroid colon and Hodgkins lymphoma.

Symptoms include muscle spasms hyper-rigidity debilitating pain and chronic anxiety. Symptoms include muscle spasms and rigidity. Muscle spasms can be so violent they can dislocate joints and even break bones.

Symptoms may include extreme muscle stiffness rigidity and painful spasms in the trunk and limbs severely impairing mobility.


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