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Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 “Janus” genetic variation

✍ Scribed by Sam W. Moore; Monique Zaahl

Book ID
116688219
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
256 KB
Volume
45
Category
Article
ISSN
0022-3468

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The multiple endocrine neoplasia type 2 (MEN2) syndromes and Hirschsprung's disease (HSCR) are inherited neurocristopathies characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, parathyroid disease, and gastrointestinal neuromatosis. Mutations in the RET proto-oncogene are the underl