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- W2106308001 abstract "La maladie de Von Recklinghausen ou neurofibromatose de type 1 (NF1) est une maladie hereditaire frequente, a transmission autosomique dominante; 50 % des cas environ sont dus a la forme sporadique (mutations de novo). Les manifestations les plus frequentes sont cutanees (tâches cafe au lait) et neurologiques (neurofibromes cutanes), mais des manifestations buccales peuvent egalement etre observees.Certaines manifestations presentent parfois une transformation maligne. Ceci exige un suivi a long terme de ces manifestations, et une prise en charge impliquant souvent l’intervention de differents specialistes dont le medecin-dentiste qui devra connaitre l’attitude therapeutique face aux patients presentant ce syndrome.Un cas d’un neurofibrome siegeant sur la face ventrale de la langue chez un patient âge de 55 ans, atteint de la maladie de Von Recklinghausen, est presente." @default.
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- W2106308001 date "2010-12-24" @default.
- W2106308001 modified "2023-09-27" @default.
- W2106308001 title "Neurofibromatose type 1 avec un neurofibrome lingual" @default.
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- W2106308001 doi "https://doi.org/10.1051/mbcb/2010045" @default.
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