Phenotypic variation in eight extended <i>CDKN2A</i> germline mutation familial atypical multiple mole melanoma–pancreatic carcinoma–prone families

Abstract

The authors suggest that these tumors may collectively, in concert with CDKN2A mutations, constitute a "new" putative hereditary carcinoma syndrome referred to as FAMMM-PC. More clinical and molecular genetic research on additional families with pancreatic carcinoma in concert with the FAMMM will be required.