A Vietnamese MEN2A syndrome patient with C634G germline mutation of the RET proto-oncogene

A Vietnamese MEN2A syndrome patient with C634G germline mutation of the RET proto-oncogene

Multiple endocrine neoplasia type 2A (MEN 2A) is a rare, autosomal dominant disease. It is characterized by complete penetrance of medullary thyroid carcinoma (MTC), lower prevalence of pheochromocytoma, hyperparathyroidism, and sometimes cutaneous lichen amyloidosis. Here, we reported a rare case o...

Full description

Bibliographic Details
Main Authors: Pham Le Bich Hang, Nguyen Thi Thanh Hoa, Dao Duc Phong, Mac Thi Thom, Nguyen Dang Ton, Le Thi Thu Hien, Nong Van Hai, Nguyen Hai Ha
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:Journal of Clinical and Translational Endocrinology Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2214624518300546

Internet

http://www.sciencedirect.com/science/article/pii/S2214624518300546

Similar Items