It is a family and hereditary disease that consists of the association of digestive polyps, especially jejunoileal, with cutaneomucosal pigment spots.
Llard, Washington +2 more
openaire +1 more source
Severe Iron Deficiency Anemia in a Jehovah's Witness diagnosed with Peutz-Jeghers Syndrome. [PDF]
Gulla V +5 more
europepmc +1 more source
Familial pediatric Peutz-Jeghers syndrome with recurrent intussusception: case report and literature review. [PDF]
Sahli S +7 more
europepmc +1 more source
Neurofibromatosis type 1 with concomitant Peutz-Jeghers syndrome in a child: a case report. [PDF]
Liu Q, Long Y.
europepmc +1 more source
A Case of Peutz-Jeghers Syndrome Complicated With Hirschsprung Disease. [PDF]
Murakawa S +5 more
europepmc +1 more source
A novel effect of bevacizumab in reducing characteristic pigmentation in Peutz-Jeghers syndrome: a case report and literature review. [PDF]
Wu D +5 more
europepmc +1 more source
Peutz-Jeghers Syndrome With Malignant Transformation in a Hamartomatous Rectal Polyp: A Case Report. [PDF]
Bahlaoui O +4 more
europepmc +1 more source
Peutz-Jegher's syndrome presenting as jejunoileal intussusception in an adult male: a case report [PDF]
Hardik H Thakker +2 more
core +1 more source
Ischemic polypectomy for small-bowel polyps in pediatric Peutz-Jeghers syndrome. [PDF]
Grabau JM, Bhatti U, Hoskins BJ.
europepmc +1 more source

