The syndrome of multiple endocrine neoplasia type IIA in three generations of one family (continued 50years of observation)
Author(s) -
Sergey Vladimirovich Sergуikо,
Valeriy A. Privalov
Publication year - 2015
Publication title -
endocrine surgery
Language(s) - English
Resource type - Journals
eISSN - 2310-3965
pISSN - 2306-3513
DOI - 10.14341/serg2015344-48
Subject(s) - multiple endocrine neoplasia , endocrine system , pheochromocytoma , medicine , cancer , hyperparathyroidism , medullary cavity , medullary thyroid cancer , thyroid cancer , genetics , biology , hormone , gene
Syndrome Sipple is the second name of the syndrome of multiple endocrine neoplasia type II (MEN2A). In 1961 J.H. Sipple described several relatives with medullary thyroid cancer, feohromotsytoma and hyperparathyroidism. The following observation is presented.
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