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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Detaylı Bibliyografya
Asıl Yazarlar: Majidi, Mahnaz, Haghpanah, Vahid, Hedayati, Mahdi, Khashayar, Patricia, Mohajeri-Tehrani, Mohammad Reza, Larijani, Bagher
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2011
Konular:
Case Report
Online Erişim: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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