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peutz jeghers syndrome		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. [ Articles | Books | Images | Discussion groups ]
Additional comments : (Perioral Lentiginosis, Polyps-and-Spots Syndrome)

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