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

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14 Citations (Scopus)

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

Dysplastic Nevus Syndrome
Nevus
Skin
Nuclear Family
Phenotype

All Science Journal Classification (ASJC) codes

  • Dermatology
  • Pediatrics, Perinatology, and Child Health

Cite this

The cutaneous evolution of nevi in a patient with familial, atypical, multiple-mole melanoma syndrome. / Lynch, Henry T.; Fusaro, R. M.; Treger, C. L.; Pester, J.

In: Pediatric Dermatology, Vol. 2, No. 4, 1985, p. 289-293.

Research output: Contribution to journalArticle

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