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https://dspace.ctu.edu.vn/jspui/handle/123456789/43119
Title: | Genetic testing identifies the potential risk of multiple endocrine neoplasia in a Vietnamese family |
Authors: | Nguyen, Hai Ha Nguyen, Thi Thanh Hoa Pham, Thi Dung Nguyen, Huy Binh Nguyen, Dang Ton |
Keywords: | Multiple Endocrine Neoplasia 2A RET Proto-oncogene P.C634R mutation |
Issue Date: | 2020 |
Series/Report no.: | Journal of Biotechnology;Vol. 18, No. 02 .- P.223-229 |
Abstract: | Multiple endocrine neoplasia type 2A (MEN2A) is a rare syndrome characterized by the presence of medullary thyroid carcinoma, pheochromocytoma, hyperparathyroidism and sometimes cutaneous lichen amyloidosis. This syndrome is caused by a germline activation mutation in the rearranged during transfection (RET) proto-oncogene transmitted by an autosomal dominant inheritance. In this study, wc reported a rare case of a 44-year-old man from Vietnam with medullary thyroid carcinoma and pheochromocytoma as the symptom of MEN2A. |
URI: | https://dspace.ctu.edu.vn/jspui/handle/123456789/43119 |
ISSN: | 1811-4989 |
Appears in Collections: | Công nghệ sinh học |
Files in This Item:
File | Description | Size | Format | |
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_file_ Restricted Access | 1.99 MB | Adobe PDF | ||
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