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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Autors principals: Ha, Minsu, Chung, Jun Won, Hahm, Ki Baik, Kim, Yoon Jae, Lee, Woochang, An, Jungsuk, Kim, Dong Kyu, Kim, Myeong Gun
Format: Artigo
Idioma:Inglês
Publicat: Baishideng Publishing Group Co., Limited 2012
Matèries:
Case Report
Accés en línia: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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