Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: clinical features, genetics and surveillance recommendations in childhood

Children and adolescents who present with neuroendocrine tumors are at extremely high likelihood of having an underlying germline predisposition for the Multiple Endocrine Neoplasia (MEN) syndromes, including MEN1, MEN2A and B, MEN4, and Hyperparathyroid-Jaw Tumor (HPT-JT) Syndromes. Each of these a...

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Detalhes bibliográficos
Publicado no:Clin Cancer Res
Main Authors: Wasserman, Jonathan D., Tomlinson, Gail E., Druker, Harriet, Kamihara, Junne, Kohlmann, Wendy K., Kratz, Christian P., Nathanson, Katherine L., Pajtler, Kristian W., Parareda, Andreu, Rednam, Surya P., States, Lisa J., Villani, Anita, Walsh, Michael F., Zelley, Kristin, Schiffman, Joshua D.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5547889/
https://ncbi.nlm.nih.gov/pubmed/28674121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1078-0432.CCR-17-0548
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