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Familial atypical multiple mole-melanoma syndrome.
Journal of Medical Genetics · 1978 · Vol. 15(5) · pp. 352–356
Henry T. Lynch✉(Creighton University)B C Frichot(Creighton University)J. F. Lynch(Creighton University)
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.
Parasitic Diseases Research and TreatmentDermatological diseases and infestationsCutaneous Melanoma Detection and ManagementConcordancePhenotypeMelanomaGeneticsBiologyMedicineGene
MeSH terms
AdultFemaleGenes, DominantHumansMaleMelanomaNevusPedigreePhenotypeSkin NeoplasmsSyndrome
Citations
380
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4.57
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18
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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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