A family presenting with multiple endocrine neoplasia type 2B: A case report

INTRODUCTION: Multiple endocrine neoplasia 2B, a rare autosomal dominant syndrome, is characterized by early onset of medullary thyroid carcinoma, pheochromocytoma, marfanoid habitus and mucosal neuromas of the tongue, lips, inner cheeks and inner eyelids. Gangliomatosis of the gastrointestinal trac...

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Detalles Bibliográficos
Autores principales: Majidi, Mahnaz, Haghpanah, Vahid, Hedayati, Mahdi, Khashayar, Patricia, Mohajeri-Tehrani, Mohammad Reza, Larijani, Bagher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287411/
https://www.ncbi.nlm.nih.gov/pubmed/22185228
http://dx.doi.org/10.1186/1752-1947-5-587

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