The Cutaneous Evolution of Nevi in a Patient with Familial, Atypical, Multiple‐mole Melanoma Syndrome
- 1 July 1985
- journal article
- case report
- Published by Wiley in Pediatric Dermatology
- Vol. 2 (4) , 289-293
- https://doi.org/10.1111/j.1525-1470.1985.tb00467.x
Abstract
For almost two decades we have followed a kindred with the familial, arypical, multiple‐mole menlanoma (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.Keywords
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