A Case of Acute Motor Axonal Type Guillain-Barr Syndrome with Anti-GM1 Antibody and Anti-GD1 Antibody. |
Tae Hong Kim, Nam Cheol Cho, Hyun Woo Park, Jae Kwan Cha, Kyu Geun Hwang |
1Department of Pediatrics, College of Medicine, Dong-a University, Pusan, Korea. 2Department of Neurology, College of Medicine, Dong-a University, Pusan, Korea. |
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Abstract |
Acute motor axonal Guillain-Barr syndrome is a paralytic disorder of abrupt onset, characterized electrophysiologically by near-normal terminal latencies, preserved nerve conduction velocity with low CAMP amplitude without a conduction block, and early appearing nerve inexcitability and by sparing sensory fibers. Most cases have antecedental infection with Campylobacter jejuni and have antibodies directed toward GM1 ganglioside-like epitopes. We have experienced a case of primary axonal type of Guillain-Barr syndrome in a 14-year-old female patient, who has symptoms of difficulty in swallowing and progressive flaccid paralysis associated with anti-GM1 antibody and anti-GD1 antibody. |
Key Words:
Acute axonal Guillain-Barr syndrome, Anti-GM1 antibody, Anti-GD1 antibody |
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