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Medullary thyroid carcinoma. MEN2A

A Family Diagnosed as MEN2A with a Rare Mutation D631Y in RET Oncogene

DOI: 
10.7727/wimj.2016.231
Synopsis: 
Mutations in the RET proto-oncogene are well documented as the genetic cause of multiple endocrine neoplasia type 2A (MEN2A) and familial medullary thyroid carcinoma (FMTC). Herein, we report a rare mutation of the RET gene (D631Y) in a Turkish family with MEN 2A.

ABSTRACT

Accepted: 
30 Jun, 2016
PDF Attachment: 
Journal Sections: 
e-Published: 19 Jul, 2016

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