A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New RET Germline Deletion

BACKGROUND: Multiple endocrine neoplasia type 2 (MEN2) is a hereditary cancer syndrome caused by RET proto-oncogene mutation. Two different clinical variants of MEN2 are known (MEN2A and MEN2B): medullary thyroid carcinoma (MTC) almost always present and associated with pheochromocytoma (Pheo), and...

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Bibliografiska uppgifter
I publikationen:Case Rep Endocrinol
Huvudupphovsmän: Giani, Carlotta, Ramone, Teresa, Romei, Cristina, Ciampi, Raffaele, Tacito, Alessia, Valerio, Laura, Agate, Laura, Ugolini, Clara, Marinò, Michele, Basolo, Fulvio, Franchi, Alessandro, Borsari, Simona, Michelucci, Angela, Selli, Cesare, Materazzi, Gabriele, Cetani, Filomena, Elisei, Rossella
Materialtyp: Artigo
Språk:Inglês
Publicerad: Hindawi 2020
Ämnen:
Case Report
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7411486/
https://ncbi.nlm.nih.gov/pubmed/32802527
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/4147097
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