Chronic Inflammatory Demyelinating Polyneuropathy [CIDP]

Authors

  • Simranjit Singh Department of Clinical Medicine, Indiana University School of Medicine, Indianapolis, IN, USA Author
  • Fnu Sanna Department of Clinical Medicine, Indiana University School of Medicine, Indianapolis, IN, USA Author
  • Jashan J S Dhaliwal Manipal College of Medical Sciences, Pokhara, Nepal Author

DOI:

https://doi.org/10.47363/JMHC/2022(4)196

Keywords:

Polyneuropathy [CIDP], Demyelinating, Inflammatory, Chronic

Abstract

Chronic Inflammatory Demyelinating Polyneuropathy [CIDP] is the most common autoimmune polyneuropathy in adults. It is characterized by weakness in both proximal and distal muscle groups, areflexia, slower onset [greater than 8 weeks], electrodiagnostic features of conduction block with asymmetric conduction velocity slowing, and cytoalbuminologic dissociation [elevated CSF protein without pleocytosis] [1]. Electrodiagnostic studies in acquired demyelination are consistent with conduction block which shows a decreasing amplitude of the compound muscle action potential [CMAP] at more proximal stimulation sites

Author Biographies

  • Simranjit Singh, Department of Clinical Medicine, Indiana University School of Medicine, Indianapolis, IN, USA

    Department of Clinical Medicine, Indiana University School of Medicine, Indianapolis, IN, USA

  • Fnu Sanna, Department of Clinical Medicine, Indiana University School of Medicine, Indianapolis, IN, USA

    Department of Clinical Medicine, Indiana University School of Medicine, Indianapolis, IN, USA

  • Jashan J S Dhaliwal, Manipal College of Medical Sciences, Pokhara, Nepal

    Manipal College of Medical Sciences, Pokhara, Nepal

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Published

2022-06-09