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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Dades bibliogràfiques
Autors principals: Majidi, Mahnaz, Haghpanah, Vahid, Hedayati, Mahdi, Khashayar, Patricia, Mohajeri-Tehrani, Mohammad Reza, Larijani, Bagher
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2011
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3287411/
https://ncbi.nlm.nih.gov/pubmed/22185228
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-5-587
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