[Miller Fischer syndrome: about a paediatric case].
Autor: | Khiri N; Service de Réanimation, CHU Mohamed VI, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed 1 Oujda, Maroc., Lazreg M; Service de Réanimation, CHU Mohamed VI, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed 1 Oujda, Maroc., Bkiyar H; Service de Réanimation, CHU Mohamed VI, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed 1 Oujda, Maroc., Diyas S; Service de Réanimation, CHU Mohamed VI, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed 1 Oujda, Maroc., Housni B; Service de Réanimation, CHU Mohamed VI, Faculté de Médecine et de Pharmacie d'Oujda, Université Mohammed 1 Oujda, Maroc. |
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Jazyk: | francouzština |
Zdroj: | The Pan African medical journal [Pan Afr Med J] 2018 May 17; Vol. 30, pp. 37. Date of Electronic Publication: 2018 May 17 (Print Publication: 2018). |
DOI: | 10.11604/pamj.2018.30.37.14136 |
Abstrakt: | Miller Fischer (MF) syndrome is a rare variant of Guillain-Barré syndrome which occurs only in 5% of cases among adults while the pediatric cases described in the literature are even more rare. We here report the case of a 12-year old boy who was diagnosed with Miller Fischer syndrome based on clinical presentation characterized by obvious ocular involvement and anti-ganglioside antibody-positivity. The patient was admitted to our hospital with respiratory distress requiring orotracheal intubation and intravenous immunoglobulins, with good clinical evolution. |
Databáze: | MEDLINE |
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