When inherited, Peutz-Jeghers syndrome is transmitted as an autosomal dominant trait. This means that, on average, each child of someone with familial PJS has a 50-50 chance of inheriting PJS.

• A family history of Peutz-Jeghers syndrome
• Dark freckles on and around the lips of a newborn
• Brownish or bluish-gray pigmented spots on the lips, gums and inner lining of the mouth
• Crampy abdominal pain, vomiting
• Occasional visible blood in the stool

• Intestinal polyps
• Intussusception (part of the intestine folds in on itself)
• Clubbed fingers or toes
• Exostoses (benign tumors in the ear)
• Anemia

Tests

• Genetic testing
• X-ray of abdomen to detect intestinal polyps
• Stool guaiac (a test for blood in the stool)
• Complete blood count (CBC)
• Total iron-binding capacity (TIBC) (a blood test)
• Polyps biopsy (colonoscopy or flexible sigmoidoscopy)

Surgery may be needed to remove polyps that cause chronic problems. Iron supplements help counteract blood loss.

In addition, the patient should be monitored periodically to watch for malignant changes in polyps. Comprehensive surveillance guidelines can be found at geneclinics.org. A booklet with additional information by Johns Hopkins University is available at hopkins-coloncancer.org.

An electronic mailing list (discussion group) is available at acor.org.

The outcome varies depending on what problems develop.

• Intussusception (part if the intestine folds in on itself)
• Polyps that lead to cancer
• Ovarian cysts
• Sex cord tumors

Call for an appointment with your health care provider if symptoms of this condition are present. Severe abdominal pain indicates a possible emergency condition such as intussusception.

If you are planning to have children and there is a family history of this condition, it may be helpful to talk with your health care provider.

Genetic counseling is recommended for prospective parents with a family history of Peutz-Jeghers syndrome. Genetic counselors can be located through the Cancer Genetics Services Directory.