A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New RET Germlin...
A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New RET Germline Deletion
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Author / Creator
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 and Elisei, Rossella
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Language
English
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BACKGROUNDMultiple 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 primary hyperparathyroidism (HPTH) in MEN2A and with...
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Full title
A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New RET Germline Deletion
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Record Identifier
TN_cdi_proquest_miscellaneous_2434748628
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2434748628
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ISSN
2090-6501
DOI
10.1155/2020/4147097
