Syndrome de Miller-Fischer, anticorps anti-GQ 1b et Campylobacter jejuni: à l'occasion d'une observation

Laplatte, G.; Bouterra, C; A, Itani; Kuteifan, Khaldoun; Gutbub, A. M.

doi:10.1016/s1164-6756(00)90010-0

Cited by 2 publications

(1 citation statement)

References 6 publications

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“…But, the involvement of the cranial nerves seems to be the most frequent in the forms of MFS-GBS overlap: facial nerve in 30 to 50% of cases [2,7,8], bulbar cranial nerves, glossopharyngeal (IX), wave ( X), large hypoglossus (XII), responsible for disorders of swallowing and dysphonia, in 13% of cases [2,7,9]. Cases of MFS with optic neuropathy (10), quadriplegia, respiratory disease or dysautonomic manifestations (5) are exceptional.…”

Section: Discussionmentioning

confidence: 99%

Miller-fisher syndrome on the borders of guillain-barre syndrome: about one case and review of literature

Labodi¹,

Adrien²,

Anne³

et al. 2017

Clin Med Rep

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Miller-Fisher syndrome combines the clinical trial, ophthalmoplegia, ataxia, and diffuse osteotendinous areflexia. It is a variant of Guillain-Barré syndrome, from which it differs by the positivity of anti-GQIb antibodies in the serum. Its clinical evolution is most often favorable. In addition to the classical form, exceptional clinical forms, either incomplete or extended to the confines of the SGB are also described. We thus describe a case of extensive SMF, overlapping with the SGB, associating in addition to the classical triad, bulbar, facial and dysautonomic involvement, of rapidly favorable evolution after a polyvalent immunoglobulin treatment in intravenous, in a man French 47-year-old.

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