Peutz-Jeghers Syndrome


Hamartomatous Intestinal Polyposes

Hamartomatous Intestinal Polyposis

Intestinal Polyposes, Hamartomatous

Intestinal Polyposis, Hamartomatous

Lentiginoses, Perioral

Lentiginosis, Perioral

Perioral Lentiginoses

Perioral Lentiginosis

Periorificial Lentiginosis Syndrome

Periorificial Lentiginosis Syndromes

Peutz Jegher's Syndrome

Peutz Jeghers Polyposis

Peutz Jeghers Syndrome

Peutz-Jegher Syndrome

Peutz-Jegher's Syndrome

Peutz-Jeghers Polyposis

Polyposes, Hamartomatous Intestinal

Polyposis, Hamartomatous Intestinal

Polyposis, Peutz-Jeghers

Polyps and Spots Syndrome

Polyps-and-Spots Syndrome

Polyps-and-Spots Syndromes

Syndrome, Periorificial Lentiginosis

Syndrome, Peutz-Jegher's

Syndrome, Peutz-Jeghers

Syndrome, Polyps-and-Spots

Syndromes, Periorificial Lentiginosis

Syndromes, Polyps-and-Spots

A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.