Multiple endocrine neoplasia type 2

Multiple Endocrine Neoplasia Type 2 (MEN2) is a rare hereditary complex disorder characterized by the presence of medullary thyroid carcinoma (MTC), unilateral or bilateral pheochromocytoma (PHEO) and other hyperplasia and/or neoplasia of different endocrine tissues within a single patient. MEN2 has...

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Bibliografski detalji
Glavni autori: Marini, Francesca, Falchetti, Alberto, Del Monte, Francesca, Carbonell Sala, Silvia, Tognarini, Isabella, Luzi, Ettore, Brandi, Maria Luisa
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2006
Teme:
Review
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1654141/
https://ncbi.nlm.nih.gov/pubmed/17105651
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-1-45
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