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

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Ioannidis, Orestis; Papaemmanouil, Styliani; Paraskevas, George; Kotronis, Anastasios; Chatzopoulos, Stavros; Konstantara, Athina; Papadimitriou, Nikolaos; Makrantonakis, Apostolos; Kakoutis, Emmanouil;
(2012)
  • Publisher: Aran Ediciones
  • Journal: Revista Espanola de Enfermedades Digestivas (issn: 1130-0108)
  • Publisher copyright policies & self-archiving
  • Subject: Diseases of the digestive system. Gastroenterology | Enterotomy | RC799-869 | Polypectomy | Hamartomatous polyps

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 ... View more
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