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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Hlavní autoři: Majidi, Mahnaz, Haghpanah, Vahid, Hedayati, Mahdi, Khashayar, Patricia, Mohajeri-Tehrani, Mohammad Reza, Larijani, Bagher
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2011
Témata:
Case Report
On-line přístup: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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