Peutz-Jeghers syndrome

An autosomal dominant disorder caused by pathogenic variants in the STK11 gene, characterized by hamartomatous polyps in the gastrointestinal tract, mucocutaneous pigmentation and increased risk of GI and extra-GI malignancies.

Also known as: Jeghers-Peutz syndrome, PJS, Peutz Jeghers Syndrome, Peutz's syndrome, Peutz-Jeghers syndrome, STK11-related Peutz-Jeghers syndrome, hamartomatous intestinal polyposis, polyps and spots syndrome

42 clinical trials for this condition and its sub-types, 9 tagged with Peutz-Jeghers syndrome itself.