(Q1544989)

English

Peutz-Jeghers syndrome

autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis)

  • Colonic hamartomatous polyp
  • Peutz Jeghers colon polyp
  • Peutz Jeghers polyp
  • Peutz-Jeghers polyp of small Intestine
  • gastric Peutz-Jeghers polyp
  • peutz-jeghers small bowel hamartoma
  • Peutz–Jeghers syndrome

Statements

Identifiers

0 references
0 references
0 references
0 references
LD2D.0
Peutz-Jeghers syndrome
0 references
0 references
0 references
Peutz-Jeghersin oireyhtymä
Peutz-Jeghers syndrom
Peutz-Jeghers syndrome
1 reference