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L’histiocytose langerhansienne est une maladie multisystémique, responsable de symptômes variés, notamment neurologiques. Nous rapportons le cas d’une fille de 20 mois qui a présenté une histiocytose langerhansienne avec atteinte hépatique et cutanée, originale par son mode de révélation sous forme de manifestations pseudoneurologiques à type d’accès d’hypertonie du tronc, apparus dans les 2 mois...
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