A Case of Multiple Endocrine Neoplasia Type 2B and Gangliomatosis of Gastrointestinal Tract

Multiple endocrine neoplasia type 2 (MEN2) is a rare familial syndrome caused by mutations in the RET protooncogene and it is transmitted as an autosomal dominant trait. The underlying problem for all the MEN syndromes is failure of a tumour suppressor gene. The genetic defect in MEN2 is on chromoso...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Shahnazari, Banafshe, Aghamaleki, Aria, Larijani, Bagher, Mohajeri Tehrani, Mohammad Reza, Rafati, Hasan, Babamahmoodi, Abdolreza
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Hindawi Publishing Corporation 2012
Pynciau:
Case Report
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3472613/
https://ncbi.nlm.nih.gov/pubmed/23093970
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/491054
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