In 1859, Landry1 described the clinical features of acute ascending weakness without amyotrophy. Other 19th-century clinical descriptions followed, but the full extent of the motor polyradiculoneuritis and the characteristic albuminocytologic dissociation in the cerebrospinal fluid was only described in 1916 by Guillain, Barré, and Strohl.2 Guillain (1876-1961), who eventually held Charcot's Professorial Chair at the Salpiêtrière in Paris, France, encountered the syndrome in soldiers while he was chief staff physician for the Sixth Army Neurological Center at the North front in France. Over the subsequent 20 years, more than 30 such cases were documented in the international medical literature to which Guillain3 himself added 10 cases in his follow-up article of 1936. The condition became known internationally under the rubric Guillain-Barré syndrome(GBS). Although the condition was originally suspected to be infectious in nature, the distinctive pathological features led to hypotheses of immunological origin. This article cites seminal views on the syndrome and traces historical developments up to the time of Guillain's death in 1961.
Bonduelle M. Guillain-Barré Syndrome. Arch Neurol. 1998;55(11):1483–1484. doi:10.1001/archneur.55.11.1483
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