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Familial atypical multiple mole-melanoma syndrome.

Journal of Medical Genetics · 1978 · Vol. 15(5) · pp. 352–356
Henry T. LynchB C FrichotJ. F. Lynch

Abstract

A family is described showing concordance for malignant melanoma and a cutaneous phenotype characterised by multiple large moles of variable size and colour (reddish-brown to bright red) with pigmentary leakage. Transmission of the cutaneous phenotype in the subject family, and in several others currently under investigation, shows an inheritance pattern consistent with a simple autosomal dominant factor. This cutaneous phenotype signifying melanoma risk may now be added to an increasing body of knowledge dealing with cancer-related genodermatoses.

MeSH terms

AdultFemaleGenes, DominantHumansMaleMelanomaNevusPedigreePhenotypeSkin NeoplasmsSyndrome
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Familial atypical multiple mole-melanoma syndrome.
Journal of Medical Genetics · 1978 · 380 citations
References
Familial atypical multiple mole-melanoma syndrome.
Journal of Medical Genetics · 1978 · 380 citations
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