Peutz-Jeghers syndrome natural history, complications, and prognosis
Peutz-Jeghers syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Peutz-Jeghers syndrome natural history, complications, and prognosis On the Web |
American Roentgen Ray Society Images of Peutz-Jeghers syndrome natural history, complications, and prognosis |
FDA on Peutz-Jeghers syndrome natural history, complications, and prognosis |
CDC on Peutz-Jeghers syndrome natural history, complications, and prognosis |
Peutz-Jeghers syndrome natural history, complications, and prognosis in the news |
Blogs on Peutz-Jeghers syndrome natural history, complications, and prognosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Peutz-Jeghers, also known as Hereditary Intestinal Polyposis Syndrome, is an autosomal dominant genetic disease characterized by the development of benign hamartomatous polyps in the gastrointestinal tract.
Prognosis
Almost half of Peutz-Jeghers patients die from cancer by age 57 years, and the cumulative risk of developing a form of cancer associated with Peutz-Jeghers syndrome between ages 15-64 is 93%.[1]
References
- ↑ "eMedicine - Peutz-Jeghers Syndrome : Article by Andrea Duchini, MD". Retrieved 2007-07-21.
Template:Digestive system neoplasia
de:Peutz-Jeghers-Syndrom
it:Sindrome di Peutz-Jeghers
nl:Syndroom van Peutz-Jeghers