Genetic counseling in melanoma

Author

Badenas Orquin, Celia

Aguilera, Paula

Puig Butillé, Joan Anton

Carrera Álvarez, Cristina

Malvehy, J. (Josep)

Puig i Sardà, Susana

Publication date

2019-02-05T14:06:32Z

2019-02-05T14:06:32Z

2012-10

2019-02-05T14:06:32Z

Abstract

Genetic counseling may be offered to families with melanoma and to individuals with multiple melanomas to better understand the genetic susceptibility of the disease, the influence of environmental factors, the inheritance of the risk, and behavior that decreases the risk of dying from melanoma, including specific dermatological follow‐up such as total body photography and digital dermoscopy. Genetic testing may be offered to those individuals with more than a 10% chance of being a carrier of a mutation. This risk varies according to the incidence of melanoma in the country and sun behavior. In countries with a low‐medium incidence of melanoma, genetic testing should be offered to families with two cases of melanoma or an individual with two primary melanomas. In countries with a high incidence, families with three cases of melanoma, with two melanomas and one pancreatic adenocarcinoma, or patients with three primary melanomas, may benefit from genetic testing.

Document Type

Article
Accepted version

Language

English

Subjects and keywords

Melanoma; Genètica; Melanoma; Genetics

Publisher

Wiley

Related items

Versió postprint del document publicat a: https://doi.org/10.1111/j.1529-8019.2012.01499.x

Dermatologic Therapy, 2012, vol. 25, num. 5, p. 397-402

https://doi.org/10.1111/j.1529-8019.2012.01499.x

Rights

(c) Wiley, 2012