The Candle Spot: An Unreported Sign of SULT2B1-nEDD

Authors

  • Sarah Milesi Departement of Dermatology, CHU Toulouse, Toulouse, France https://orcid.org/0009-0000-0638-8315
  • Christine Chiaverini Departement of Dermatology, CHU Nice, Nice, France
  • Laura Chêne Departement of Dermatology, CHU Nice, Nice, France
  • Nathalie Jonca Toulouse Institute for Infectious and Inflammatory Diseases (INFINITy), Toulouse University, CNRS, Inserm, Toulouse, France; Department of Cell Biology and Cytology, Federative Institute of Biology, Purpan University Hospital, Toulouse, France
  • Juliette Mazereeuw-Hautier Departement of Dermatology, CHU Toulouse, Toulouse, France,

DOI:

https://doi.org/10.2340/actadv.v106.adv-2025-0264

Keywords:

ichthyosis, SULT2B1, SULT2B1a protein human, nEDD

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References

Hernández-Martín Á, Paller AS, Sprecher E, Akiyama M, Granier Tournier C, Aldwin-Easton M, et al. A proposal for a new pathogenesis-guided classification for inherited epidermal differentiation disorders. Br J Dermatol 2025; 193: 544–548. DOI: https://doi.org/10.1093/bjd/ljaf065

Heinz L, Kim GJ, Marrakchi S, Christiansen J, Turki H, Rauschendorf MA, et al. Mutations in SULT2B1 cause autosomal-recessive congenital ichthyosis in humans. Am J Hum Genet 2017; 100: 926–939. DOI: https://doi.org/10.1016/j.ajhg.2017.05.007

Fozia F, Nazli R, Alam Khan S, Bari A, Nasir A, Ullah R, et al. Novel homozygous mutations in the genes TGM1, SULT2B1, SPINK5 and FLG in four families underlying congenital ichthyosis. Genes 2013; 12: 373. DOI: https://doi.org/10.3390/genes12030373

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Published

2026-06-01

How to Cite

Milesi, S., Chiaverini, C., Chêne, L., Jonca, N., & Mazereeuw-Hautier, J. (2026). The Candle Spot: An Unreported Sign of SULT2B1-nEDD. Acta Dermato-Venereologica, 106, adv–2025. https://doi.org/10.2340/actadv.v106.adv-2025-0264

Issue

Vol. 106 (2026)

Section

Short Communication

License

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