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Original Article
Two Cases of Peutz-Jeghers Syndrome.
Joo Saeng Moon, Sung Ki Jin, Doo Sung Moon, Kyung Sook Cho, Jong Dase Cho
Clin Exp Pediatr. 1987;30(8):907-915.   Published online August 31, 1987
Peutz-Jeghers syndrome is characterized by hamartomtous polyps of the gastrointestinal tract (stomach, small bowel, and colon) and mucocutaneous pigmentation (lips, oral mucosa, fingers, forearms, toes and umbilical area). About 50% of the reported cases have a positive family history of autosomal dominant mode of inheritacnce, whereas the remaining 50% are sporadic. We have experienced two case of Peutz-Jeghers syndrome with no definite family history....


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