Recurrent small intestine intussusception in a patient with Peutz-Jeghers syndrome Invaginación recurrente del intestino delgado en un paciente con síndrome de Pentz-Jeghers

Recurrent small intestine intussusception in a patient with Peutz-Jeghers syndrome Invaginación recurrente del intestino delgado en un paciente con síndrome de Pentz-Jeghers

Peutz-Jeghers syndrome is a rare hereditary autosomal dominant disease caused by a mutation of the tumor suppressor gene serine/threonine kinase 11 located in chromosome 19p13.3. It is characterized by the presence of extensive mucocutaneous pigmentation, especially of the lips and the occurrence of...

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Bibliographic Details
Main Authors: Orestis Ioannidis, Styliani Papaemmanouil, George Paraskevas, Anastasios Kotronis, Stavros Chatzopoulos, Athina Konstantara, Nikolaos Papadimitriou, Apostolos Makrantonakis, Emmanouil Kakoutis
Format: Article
Language:English
Published: Aran Ediciones 2012-01-01
Series:Revista Espanola de Enfermedades Digestivas
Subjects:
Enterotomy
Polypectomy
Hamartomatous polyps
Online Access:http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082012000100009

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http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082012000100009

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