What is Familial Atypical Multiple Mole Melanoma Syndrome?
Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome is a genetic condition characterized by the presence of multiple atypical moles (nevi) and a higher risk of developing melanoma, a type of skin cancer. Individuals with FAMMM syndrome typically have a family history of melanoma and multiple atypical moles. The condition is inherited in an autosomal dominant pattern, meaning a single copy of the altered gene in each cell is sufficient to increase the risk of developing melanoma.
