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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Detalhes bibliográficos
Principais autores: Ha, Minsu, Chung, Jun Won, Hahm, Ki Baik, Kim, Yoon Jae, Lee, Woochang, An, Jungsuk, Kim, Dong Kyu, Kim, Myeong Gun
Formato: Artigo
Idioma:Inglês
Publicado em: Baishideng Publishing Group Co., Limited 2012
Assuntos:
Case Report
Acesso em linha: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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