GENETICS OF FAMILIAL ATYPICAL MULTIPLE MOLE-MELANOMA (FAMMM) SYNDROMEIN THE NETHERLANDS - HOW FAR HAVE WE COME

Citation
Na. Gruis et al., GENETICS OF FAMILIAL ATYPICAL MULTIPLE MOLE-MELANOMA (FAMMM) SYNDROMEIN THE NETHERLANDS - HOW FAR HAVE WE COME, Bulletin du cancer, 85(7), 1998, pp. 627-630
Citations number
32
Categorie Soggetti
Oncology
Journal title
ISSN journal
00074551
Volume
85
Issue
7
Year of publication
1998
Pages
627 - 630
Database
ISI
SICI code
0007-4551(1998)85:7<627:GOFAMM>2.0.ZU;2-7
Abstract
By the genetic localization of the first melanoma susceptibility gene on chromosome 1p we thought that the puzzle on familial melanoma famil ies would soon be solved. Now, almost fifteen years later we have lear ned that inherited melanoma is not a simple genetic disorder and that multiple genes, modifying genes and environmental factors might be inv olved. This paper outlines the current understanding of the genetics o f melanoma and the relationship to atypical nevi based on more than te n years of genetic analysis in the Dutch familial atypical multiple mo le-melanoma (FAMMM) syndrome families.