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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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Detalhes bibliográficos
Main Authors: Çetin, Deniz, Ünübol, Mustafa, Soyder, Aykut, Güney, Engin, Coşkun, Adil, Özbaş, Serdar, Ünsal, Alparslan, Erkuş, Muhan
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3483661/
https://ncbi.nlm.nih.gov/pubmed/23119190
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/360328
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