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- W3048851223 abstract "Le syndrome de Sturge-Weber (SWS) ou angiomatose encéphalo-faciale, est un syndrome neuro-cutané et oculaire congénital rare. Il comporte deux types de malformations: capillaire faciale congénitale à type d´angiome plan et capillaro-veineux lepto-méningé de localisation le plus souvent pariéto-occipitale homolatérale. La Neuroimagerie, essentiellement l´imagerie par résonnance magnétique (IRM), joue un rôle important dans l'établissement du diagnostic, idéalement avant l'apparition de complications neuro-oculaires. Nous rapportons le cas d´un enfant chez qui le SWS est suspecté devant la présence d´un angiome facial et d´une épilepsie pharmaco-résistante." @default.
- W3048851223 created "2020-08-18" @default.
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- W3048851223 date "2020-01-01" @default.
- W3048851223 modified "2023-09-23" @default.
- W3048851223 title "Le syndrome Sturge-Weber: à propos d'un cas" @default.
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- W3048851223 doi "https://doi.org/10.11604/pamj.2020.36.273.24346" @default.
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