Please use this identifier to cite or link to this item: 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

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