The cutaneous evolution of nevi in a patient with familial, atypical, multiple-mole melanoma syndrome

Henry T. Lynch, R. M. Fusaro, C. L. Treger, J. Pester

Research output: Contribution to journalArticle

14 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)289-293
Number of pages5
JournalPediatric Dermatology
Volume2
Issue number4
StatePublished - 1985

    Fingerprint

All Science Journal Classification (ASJC) codes

  • Dermatology
  • Pediatrics, Perinatology, and Child Health

Cite this

Lynch, H. T., Fusaro, R. M., Treger, C. L., & Pester, J. (1985). The cutaneous evolution of nevi in a patient with familial, atypical, multiple-mole melanoma syndrome. Pediatric Dermatology, 2(4), 289-293.