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pro vyhledávání: '"C. Nalini Mohan"'
Publikováno v:
Bali Medical Journal, Vol 4, Iss 2, Pp 98-101 (2015)
Background: Peutz-Jeghers syndrome is a rare genetic disorder presenting in young age with mucocutaneous pigmentation and hamartomatous polyposis. Method: We report a case of Peutz-Jeghers syndrome in a 16 year old boy presenting with acute intestina