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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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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Baishideng Publishing Group Co., Limited
2012
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| Schlagworte: | |
| Online Zugang: | 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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