CLINICAL VISTAS among 72 patients with PJS the relative risk of dying from a
gastrointestinal cancer was 13-fold greater than that in the general population and the …

Discussion: PJS is a rare autosomal dominant disorder that often remain undiagnosed for
many years. Acute complications such as intestinal obstruction secondary to intussusception …

A 20-year-old female patient with a family history significant for Peutz-Jeghers syndrome
presented to the hospital multiple times with complaints of abdominal pain. On the initial visit …

OBJECTIVES: Peutz–Jeghers syndrome (PJS) is characterized by gastrointestinal
hamartomas. The hamartomas are located predominantly in the small intestine and may …

There are two main problems in the clinical management of the gastrointestinal (GI) tract in
patients with Peutz-Jeghers syndrome (PJS), namely long-term cancer risk and managing …

Peutz-Jeghers syndrome is an autosomal dominant inherited medical condition
characterized by hyperpigmented mucocutaneous macules, hamartomatous polyps in the …

BACKGROUND Peutz-Jeghers syndrome (PJS) is a clinically rare disease with pigmented
spots on the lips and mucous membranes and extremities, scattered gastrointestinal polyps …

Peutz–Jeghers syndrome (PJS) is an autosomal dominant condition characterized by the
association of gastrointestinal polyposis, mucocutaneous pigmentation and cancer …

Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder characterized
by intestinal hamartomatous polyps in association with mucocutaneous pigmentations. Main …

Peutz–Jeghers syndrome is an uncommon genetic defect in the signal pathways of growth.
The incidence has most recently been estimated to be in the range of 1 per 120,000 live …