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

Scopus Q Değeri

Cilt

26

Sayı

1

Künye