Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?

Bull Cancer. 1998 Jul;85(7):627-30.

Abstract

By the genetic localization of the first melanoma susceptibility gene on chromosome 1p we thought that the puzzle on familial melanoma families would soon be solved. Now, almost fifteen years later we have learned that inherited melanoma is not a simple genetic disorder and that multiple genes, modifying genes and environmental factors might be involved. This paper outlines the current understanding of the genetics of melanoma and the relationship to atypical nevi based on more than ten years of genetic analysis in the Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families.

MeSH terms

  • Chromosomes, Human, Pair 1 / genetics
  • Chromosomes, Human, Pair 9 / genetics
  • Cyclin-Dependent Kinase Inhibitor p16 / genetics*
  • Cytochrome Reductases / genetics*
  • Cytochrome-B(5) Reductase
  • Genetic Linkage
  • Humans
  • Melanoma / genetics*
  • Melanoma / pathology
  • Neoplasm Proteins / genetics*
  • Neoplastic Syndromes, Hereditary / genetics*
  • Neoplastic Syndromes, Hereditary / pathology
  • Netherlands
  • Pedigree
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology

Substances

  • Cyclin-Dependent Kinase Inhibitor p16
  • Neoplasm Proteins
  • Cytochrome Reductases
  • Cytochrome-B(5) Reductase