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April 15, 2026British Journal of Dermatology0 citations

Genotype- dermatological phenotype correlations in CDKN2A , POT1 , POLE , BAP1 variant carriers using 3D total-body-imaging

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EMEllie J. MaasThe University of QueenslandSKSam KahlerThe University of QueenslandBBBrigid Betz‐StableinThe University of Queensland

Key Points

  • The study aims to characterize the relationship between genetic variants and dermatological features in melanoma susceptibility.
  • Utilized 3D total-body imaging for objective assessment of naevus characteristics.
  • Characterized naevus burden, size, and distribution in carriers and controls.
  • Compared phenotypic data between variant carriers and unaffected controls.
  • Identified increased naevus counts in carriers of POT1 and POLE variants.
  • Noted distinct, gene-specific dermatological phenotypes among variant carriers.
  • Established objective phenotypic markers relevant for melanoma risk assessment.

Abstract

This international study uses 3D total-body imaging to provide the first objective genotype–phenotype characterisation of naevus burden, size, and anatomical distribution in carriers of CDKN2A, POT1, POLE, and BAP1 variants. We identify distinct, gene-specific dermatological phenotypes, particularly increased naevus counts in POT1 and POLE carriers that are largely independent of ultraviolet damage, distinguishing variant carriers from controls. These findings establish objective phenotypic markers of inherited melanoma susceptibility with direct relevance for risk stratification and targeted genetic testing in clinical practice.

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Cite This Study

Maas et al. (2026) studied this question.

synapsesocial.com/papers/69df2b2ce4eeef8a2a6b00f7https://doi.org/10.1093/bjd/ljag137
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