Lynch H T, Fusaro R M, Treger C L, Pester J, Lynch J F
Pediatr Dermatol. 1985 Jul;2(4):289-93. doi: 10.1111/j.1525-1470.1985.tb00467.x.
For almost two decades we have followed a kindred with the familial, atypical, multiple-mole melanoma (FAMMM) syndrome. We first evaluated the proband's 14-year-old daughter when she was age 5 years. We documented the evolution, both clinically and histologically, of the FAMMM phenotype in this girl for eight years.
