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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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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Hindawi Publishing Corporation
2012
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| Schlagworte: | |
| Online Zugang: | 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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