Coexistence of Multiple Endocrine Neoplasia Type 2B and Chilaiditi Sign: A Case Report

We present a 15-year-old female patient with medullary thyroid carcinoma, marfanoid habitus, and mucosal ganglioneuromatosis. Our case had a RET protooncogene mutation ser836 polymorphism in exon 14 and ser904 polymorphism in exon 15. Our patient is thought to be atypical MEN2B due to the absence of...

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Bibliographic Details
Main Authors: Deniz Çetin, Mustafa Ünübol, Aykut Soyder, Engin Güney, Adil Coşkun, Serdar Özbaş, Alparslan Ünsal, Muhan Erkuş
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Case Reports in Endocrinology
Online Access:http://dx.doi.org/10.1155/2012/360328

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