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Cowden's disease--a report on the first case in Korea and literature review

Lee HR, Moon YS, Yeom CH, Kim KW, Chun JY, Kim HK, Choi HS, Kim DK, Chung TS

Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucocutaneous lesions associated with abnormalities of the breast, thyroid, and gastrointestinal tract. We describe a 32-year-old man...
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A Case of Crohn's Disease Accompanied by Peutz-Jeghers Syndrome

Um YJ, Kim SM, Pyo JS, Lee JA, Koo HS, Huh KC

Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by multiple gastrointestinal hamartomatous polyps and mucocutaneous pigmentation. Peutz-Jeghers syndrome has an incidence of approximately 1 in 25,000 to 300,000 births....
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