Stiff-person syndrome (SPS) is a rare neurological disorder that is characterized by progressive muscle stiffness and spasms, particularly in the trunk and limbs.
These muscle spasms can be severe and can cause difficulty with movement and mobility. SPS is thought to be an autoimmune disorder, in which the immune system mistakenly attacks healthy cells in the body, including nerve cells that control muscle movement.
Symptoms of SPS can vary widely from person to person, and may include muscle stiffness and spasms, difficulty walking, changes in posture, and abnormal sensitivity to touch or sound.
SPS may also be associated with other autoimmune disorders, such as diabetes and thyroid disease. The treatment of SPS typically involves the use of medications to control muscle spasms and stiffness and may also include physical therapy and otherwise.
The diagnosis of a stiff person syndrome (SPS) can be challenging because it is a rare disorder and its symptoms can be similar to those of other neurological conditions. To diagnose SPS, doctors typically perform a thorough physical examination and medical history, including a detailed review of the patient’s symptoms. They may also order a variety of tests to help confirm the diagnosis, such as:
It is important to note that there is no specific test that can confirm a diagnosis of SPS. Instead, the diagnosis is typically made based on the presence of specific symptoms and the results of the above tests.
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