| Literature DB >> 26892652 |
Katherine J Ransohoff1, Prajakta D Jaju, Prajaka D Jaju1, Jean Y Tang1, Michele Carbone2, Sancy Leachman3, Kavita Y Sarin4.
Abstract
Phenotypic traits, such as red hair and freckling, increase melanoma risk by 2- to 3-fold. In addition, approximately 10% of melanomas are caused by inherited germline mutations that increase melanoma risk from 4- to >1000-fold. This review highlights the key genes responsible for inherited melanoma, with an emphasis on when a patient should undergo genetic testing. Many genetic syndromes associated with increased melanoma risk are also associated with an increased risk of other cancers. Identification of these high-risk patients is essential for preventive behavior reinforcement, genetic counseling, and ensuring other required cancer screenings.Entities:
Keywords: genetic syndromes; genetics; inherited cancer risk; melanoma; oncogenes; skin cancer; tumor suppressor
Mesh:
Year: 2016 PMID: 26892652 DOI: 10.1016/j.jaad.2015.09.070
Source DB: PubMed Journal: J Am Acad Dermatol ISSN: 0190-9622 Impact factor: 11.527