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Distal acquired demyelinating symmetric neuropathy associated with anti-GM1 and anti-GD1b antibodies

  • Ko, Keun Hyuk (Department of Neurology, Jeju National University School of Medicine) ;
  • Jwa, Seung-Joo (Department of Neurology, Jeju National University School of Medicine) ;
  • Park, Sung Joo (Department of Neurology, Jeju National University School of Medicine) ;
  • Kang, Sa-Yoon (Department of Neurology, Jeju National University School of Medicine)
  • Received : 2016.04.21
  • Accepted : 2016.07.25
  • Published : 2017.01.31

Abstract

Distal acquired demyelinating symmetric (DADS) neuropathy is a variant form of chronic inflammatory demyelinating polyradiculoneuropathy. A 54-year-old man presented with gait disturbance owing to weakness in both legs. Nerve conduction studies showed demyelinating sensorimotor polyneuropathy, and laboratory studies demonstrated anti-GM1 and anti-GD1b IgG antibodies, but no anti-myelin associated glycoprotein activity. We suggest that an antiganglioside antibodies assay needs to be applied when DADS neuropathy is suspected in order to improve the classification of dysimmune neuropathies.

Keywords

References

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