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J Am Acad Dermatol ; 74(3): 423-34; quiz 435-6, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26892652

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.


Subject(s)
Melanoma/epidemiology , Melanoma/genetics , Neoplastic Syndromes, Hereditary , Skin Neoplasms/epidemiology , Skin Neoplasms/genetics , Humans , Melanoma/diagnosis , Melanoma/therapy , Neoplastic Syndromes, Hereditary/diagnosis , Neoplastic Syndromes, Hereditary/epidemiology , Neoplastic Syndromes, Hereditary/therapy , Risk , Skin Neoplasms/diagnosis , Skin Neoplasms/therapy
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