| Literature DB >> 14574008 |
Abstract
Peutz-Jeghers syndrome is a rare genetic disorder characterized by mucocutaneous melanin deposition, intestinal polyposis and an increased risk of cancer, both intestinal and extra-intestinal. We describe the current status of diagnosis and the methods by which the consequences of this condition can be minimized. A surveillance program for those diagnosed is also included.Entities:
Mesh:
Year: 2001 PMID: 14574008 DOI: 10.1023/a:1013896813918
Source DB: PubMed Journal: Fam Cancer ISSN: 1389-9600 Impact factor: 2.375