Familial syndromes associated with neuroendocrine tumours

  title={Familial syndromes associated with neuroendocrine tumours},
  author={Paweł Gut and Hanna Komarowska and Agata Czarnywojtek and Joanna Walig{\'o}rska-Stachura and Maciej Bączyk and Katarzyna Ziemnicka and Jakub Fischbach and Elżbieta Wrotkowska and Marek Ruchała},
  booktitle={Contemporary oncology},
Neuroendocrine tumours may be associated with familial syndromes. At least eight inherited syndromes predisposing to endocrine neoplasia have been identified. Two of these are considered to be major factors predisposing to benign and malignant endocrine tumours, designated multiple endocrine neoplasia type 1 and type 2 (MEN1 and MEN2). Five other autosomal dominant diseases show more heterogeneous clinical patterns, such as the Carney complex, hyperparathyroidism-jaw tumour syndrome, Von Hippel… CONTINUE READING
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SEOM clinical guidelines for the treatment of renal cell carcinoma

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico • 2014
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