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Des tumeurs endocrines gastro-entéro-pancréatiques (TE GEP) peuvent être observées dans plusieurs syndromes de prédisposition héréditaire: il s’agit essentiellement de la néoplasie endocrinienne multiple de type 1 et de la maladie de von Hippel-Lindau, beaucoup plus rarement de la neurofibromatose de type 1 ou de la sclérose tubéreuse de Bourneville. Ces quatre syndromes ont en commun un mode de transmission autosomique dominant et une pénétrance élevée (16, 26).
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Cardot-Bauters, C. (2008). Syndromes de prédisposition héréditaires aux tumeurs endocrines gastro-entéro-pancréatiques. In: Tumeurs endocrines thoraciques et digestives. Springer, Paris. https://doi.org/10.1007/978-2-287-35574-5_11
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DOI: https://doi.org/10.1007/978-2-287-35574-5_11
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