2017
DOI: 10.1590/0004-282x20170093
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Guillain-Barré syndrome: celebrating a century

Abstract: A hundred years ago, Guillain, Barré and Strohl described a syndrome with a predominant motor acute or subacute polyneuritis, albumin-cytologic dissociation in the cerebrospinal fluid, and a benign course. Before them, many other authors, such as Landry, Duménil, Osler, and Grainger Stewart had described similar cases although they had not performed lumbar punctures. In this work, we outline certain features of the beginning of this famous syndrome.

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Cited by 3 publications
(3 citation statements)
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“…It has an acute or subacute beginning and is characterised by diversified levels of limb weakness or muscles with cranial nerve innervation, loss or diminished deep tendon reflexes and albuminocytologic dissociation . It is normally triggered by an acute infectious process and is a leading cause of flaccid paralysis in the world . The precise cause of the syndrome is not known, but 50–70% of the cases occur a week or two after a gastrointestinal or a respiratory infection or other immune stimulus that triggers an atypical autoimmune response that affects the peripheral nerves and their spinal roots .…”
Section: Introductionmentioning
confidence: 99%
“…It has an acute or subacute beginning and is characterised by diversified levels of limb weakness or muscles with cranial nerve innervation, loss or diminished deep tendon reflexes and albuminocytologic dissociation . It is normally triggered by an acute infectious process and is a leading cause of flaccid paralysis in the world . The precise cause of the syndrome is not known, but 50–70% of the cases occur a week or two after a gastrointestinal or a respiratory infection or other immune stimulus that triggers an atypical autoimmune response that affects the peripheral nerves and their spinal roots .…”
Section: Introductionmentioning
confidence: 99%
“…In 1916, two French Neurologists Georges Charles Guillain and Jean Alexandre Barre and French Physiologist Andre Strohl reported an original paper encountered new syndrome in two soldiers with muscle weakness, absence of deep tendon reflexes and sensory impairment and described the key diagnosis of albumincytologic disassociation in the cerebrospinal fluid along with changes in electromyography and nerve conduction studies. Both patients were managed with massage therapy and Strychnine injection and showed clinical recovery after few months [1].…”
Section: Historymentioning
confidence: 99%
“…Approximately four decades later, in honor of its investigators, the disease received the name of Guillain-Barré syndrome (GBS). 1 GBS is a peripheral polyneuropathy, characterized by starting with acute bilateral and symmetric weakness of the limbs with reduced or absent myotactic reflexes. The disease is progressive and reaches its peak in between 12 hours and 28 days, followed by a plateau and subsequent improvement in survivors.…”
Section: Introductionmentioning
confidence: 99%