A case of Cowden syndrome diagnosed from multiple gastric polyposis

Cowden syndrome is a rare autosomal dominant disorder that is characterized by multiple hamartomas in a variety of tissues and this is associated with germline mutations in the phosphatase and tensin homologue (PTEN) gene, which is the tumor suppressor gene located on chromosome 10q23.3. It is chara...

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Bibliografiske detaljer
Main Authors: Ha, Minsu, Chung, Jun Won, Hahm, Ki Baik, Kim, Yoon Jae, Lee, Woochang, An, Jungsuk, Kim, Dong Kyu, Kim, Myeong Gun
Format: Artigo
Sprog:Inglês
Udgivet: Baishideng Publishing Group Co., Limited 2012
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3286151/
https://ncbi.nlm.nih.gov/pubmed/22371648
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v18.i8.861
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