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Original Article
A Case of Peutz-Jeghers Syndrome.
Ick berm Park, Sung guen Oh, Jung suk Ko, Sang hyun Byun, Kyu chul Choeh
Clin Exp Pediatr. 1989;32(7):990-994.   Published online July 31, 1989
This is a report of our experience of Peutz-Jeghers syndrome in a 14 year old girl having family history. She was admitted with complaints of crampy abdominal pain and vomiting, and showed melanotic pigmentation on the lips, face around nose, oral mucosa around molar areas, fingers and toes. Colon study revealed multiple polyposis in colon and small bowel. In family, her father has melanotic...
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....
Case Report
A Case of Peutz-Jeghers Syndrome.
Sang Kie Kim, Choon Ho Park, Jin Heon Kim, Keun Chul Myung, Chang Soo Ra
Clin Exp Pediatr. 1985;28(6):622-626.   Published online June 30, 1985
Peutz-Jeghers syndrome, also known as intestinal polyposis II, is a familial condition characterized by the triad of (1) mucocutaneous pigmentation, (2) benign polyps occuring in any part of the intestinal tract but mainly in the jejunum, and (3) autosomal dominant inheritance. This syndrome was first reported by Peutz in 1929. Following reemphasis by Jegers in 1949, it became a definite...
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