Review of Cowden Syndrome
碩士 === 中山醫學大學 === 醫學檢驗暨生物技術學系碩士班 === 106 === Cowden Syndrome (CS) is a rare autosomal dominant inherited disease characterized by benign hamartomatous lesions. CS patients have a higher risk of mucocutaneous, thyroid, breast, gastrointestinal cancers. PTEN mutations occurred in 80% of CS patients, a...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2018
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| Online Access: | http://ndltd.ncl.edu.tw/handle/g5by38 |