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Atypical Guillain-Barré syndrome with positive anti-sulfatide, anti-GT1b, and anti-GT1a antibodies: A case report.
Tan, Fei-Fei; Liu, He-Xu; Huang, Xue-Yan; Yu, Chang-Yin; Yang, Xiao-Yan.
Afiliação
  • Tan FF; Department of Neurology, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China.
  • Liu HX; Department of Neurology, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China.
  • Huang XY; Department of Neurology, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China.
  • Yu CY; Department of Neurology, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China.
  • Yang XY; Department of Neurology, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China. 18984215060@163.com.
World J Clin Cases ; 12(20): 4372-4376, 2024 Jul 16.
Article em En | MEDLINE | ID: mdl-39015914
ABSTRACT

BACKGROUND:

The role of diverse antibodies in mediating peripheral nerve injury in Guillain-Barré syndrome (GBS) is becoming clearer, but positivity for multiple antibodies in one case is uncommon. To our knowledge, this is the first case involving GBS with positive anti-sulfatide, anti-GT1a, and anti-GT1b antibodies. CASE

SUMMARY:

A 20-year-old female patient was admitted to the hospital due to weakness of limbs for 5 d, and deterioration of the weakness and muscle aches for 1 d. The patient's limbs were weak, but the tendon reflexes in the part of the limbs were normal. There was no comorbid peripheral nociception or deep sensory dysfunction. She was diagnosed with GBS and was discharged after receiving intravenous human immunoglobulin pulse therapy.

CONCLUSION:

In this article, the clinical manifestations, neurophysiological examination, and auxiliary examination findings of a GBS patient positive for multiple antibodies were analyzed to improve the identification of the disease by clinical physicians at an early stage.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article