A 58-year-old female was admitted because of colicky abdominal pain. Physical examination revealed firm abdominal wall, increased bowel sounds and multiple pigmented macules on the lips, oral mucosa, soles and volar aspects of the fingers and toes. Hyperventilation and tetanic rigidity of the extremities were also noted. The symptoms were successfully treated by intravenous injection of butropium bromide and diazepam. Roentgenological and fiberscopic examination revealed multiple polyps in the stomach, small intestine and colon ; the small intestine was most heavily loaded with polyps. Biopsy specimen revealed only inflammatory changes. The patient had undergone a resectien of the terminal ileum with polyps 15 years previously because of il...
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by hamartomatous po...
Peutz-Jeghers syndrome (PJS) is a dominant autosomal inherited disorder characterized by intestinal ...
Peutz-Jeghers syndrome (PJS) is a genetic disease with an autosomic dominant transmission. The 40% o...
Peutz-Jeghers Syndrome (PJS) is a rare condition that tends to run in families. Diagnosis of PJS is ...
Peutz-Jeghers syndrome is characterized mainly by the presence of hamartomatous polyposis of gastroi...
Five cases of Peutz-Jeghers syndrome in one family have been studied, and a review of the history an...
Peutz-Jeghers syndrome is a rare autosomal dominant polyposis characterized by mucocutaneous pigment...
A 17-year-old man was diagnosed as Peutz-Jeghers syndrome (PJS) because of pigmented lip and multipl...
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by typical pigmente...
Two cases of malignancy affected with Peutz-Jeghers syndrome in the same family were described. The ...
Peutz Jeghers Syndrome (PJS), which was first described in 1921 by Peutz, followed by Jeghers etal i...
PubMed ID: 1991602A family affected with Peutz-Jeghers syndrome is reported with an emphasis on radi...
Peutz-Jeghers syndrome is a rare autosomal dominant disorder of hamartomatous polyposis of the gastr...
Peutz-Jeghers syndrome is a rare autosomal dominant polyposis characterized by mucocutaneous pigment...
Peutz-Jeghers syndrome is a rare inherited condition characterized by hamartomatous gastrointestinal...
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by hamartomatous po...
Peutz-Jeghers syndrome (PJS) is a dominant autosomal inherited disorder characterized by intestinal ...
Peutz-Jeghers syndrome (PJS) is a genetic disease with an autosomic dominant transmission. The 40% o...
Peutz-Jeghers Syndrome (PJS) is a rare condition that tends to run in families. Diagnosis of PJS is ...
Peutz-Jeghers syndrome is characterized mainly by the presence of hamartomatous polyposis of gastroi...
Five cases of Peutz-Jeghers syndrome in one family have been studied, and a review of the history an...
Peutz-Jeghers syndrome is a rare autosomal dominant polyposis characterized by mucocutaneous pigment...
A 17-year-old man was diagnosed as Peutz-Jeghers syndrome (PJS) because of pigmented lip and multipl...
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by typical pigmente...
Two cases of malignancy affected with Peutz-Jeghers syndrome in the same family were described. The ...
Peutz Jeghers Syndrome (PJS), which was first described in 1921 by Peutz, followed by Jeghers etal i...
PubMed ID: 1991602A family affected with Peutz-Jeghers syndrome is reported with an emphasis on radi...
Peutz-Jeghers syndrome is a rare autosomal dominant disorder of hamartomatous polyposis of the gastr...
Peutz-Jeghers syndrome is a rare autosomal dominant polyposis characterized by mucocutaneous pigment...
Peutz-Jeghers syndrome is a rare inherited condition characterized by hamartomatous gastrointestinal...
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by hamartomatous po...
Peutz-Jeghers syndrome (PJS) is a dominant autosomal inherited disorder characterized by intestinal ...
Peutz-Jeghers syndrome (PJS) is a genetic disease with an autosomic dominant transmission. The 40% o...