Peutz-Jeghers syndrome
Autoszomális domináns · About 1 in 25,000 to 1 in 280,000 people
Hamartomatous gastrointestinal polyposis with mucocutaneous pigmentation and increased risk of gastrointestinal, breast, pancreatic and gynaecological cancers.
Mit változtat a diagnózis
Surveillance endoscopy from childhood, breast, pancreatic and gynaecological screening in adulthood, and testing of relatives.
Vizsgált gének
Más néven
hamartomatous intestinal polyposis; lentiginosis, perioral; periorificial lentiginosis syndrome; Peutz Jeghers polyposis; Peutz's syndrome; PJS; polyps and spots syndrome; STK11-related Peutz-Jeghers syndrome
