Stiff Person Syndrome-The Less Common Antibody: A Case Report
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Tarih
2020
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Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Stiff Person syndrome (SPS) is a rare, disabling syndrome characterized by progressive muscle stiffness and axial rigidity. It may have an autoimmune, paraneoplasticor cryptogenic etiology. A 59-year-old woman presented with stiffness and involuntary spasms in the lower extremities. In a neurologic examination, lowerextremity and axial rigidity were revealed. Anti-glutamic acid decarboxylase antibody was negative, anti-amphiphysin was antibody positive. She was diagnosedas having SPS. The symptoms were improved after intravenous immunoglobulin and cancer therapy.
Açıklama
Anahtar Kelimeler
Kaynak
Türk Nöroloji Dergisi
WoS Q Değeri
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Cilt
26
Sayı
1