Epidermolytic ichthyosis caused by KRT10 parental cutaneous-gonadal mosaicism: a call for prospective genetic diagnosis.

International Journal of DermatologyEarly View Correspondence Epidermolytic ichthyosis caused by KRT10 parental cutaneous-gonadal mosaicism: a call for prospective genetic diagnosis Deyu Song MD, Deyu Song MD orcid.org/0000-0001-9514-0740 Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this authorFang Zhang BS, Fang Zhang BS West China School of Medicine, Sichuan University, Chengdu, ChinaSearch for more papers by this authorYusha Chen MD, Yusha Chen MD Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this authorZhongtao Li MD, Zhongtao Li MD Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this authorSheng Wang MD, Corresponding Author Sheng Wang MD [email protected] Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this author Deyu Song MD, Deyu Song MD orcid.org/0000-0001-9514-0740 Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this authorFang Zhang BS, Fang Zhang BS West China School of Medicine, Sichuan University, Chengdu, ChinaSearch for more papers by this authorYusha Chen MD, Yusha Chen MD Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this authorZhongtao Li MD, Zhongtao Li MD Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this authorSheng Wang MD, Corresponding Author Sheng Wang MD [email protected] Department of Dermatology, West China Hospital, Sichuan University, Chengdu, ChinaSearch for more papers by this author First published: 12 September 2023 https://doi.org/10.1111/ijd.16841 Conflict of interest: None. Funding source: This work was supported by the China Postdoctoral Science Foundation (2020M683318) and Post-Doctor Research Project, West China Hospital, Sichuan University (2020HXBH029). Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1Paller AS, Syder AJ, Chan YM, Yu QC, Hutton E, Tadini G, et al. Genetic and clinical mosaicism in a type of epidermal nevus. N Engl J Med. 1994; 331: 1408–1415. 2Kono M, Suga Y, Akashi T, Ito Y, Takeichi T, Muro Y, et al. A child with epidermolytic ichthyosis from a parent with epidermolytic nevus: risk evaluation of transmission from mosaic to germline. J Invest Dermatol. 2017; 137: 2024–2026. 3Kinsler VA, Boccara O, Fraitag S, Torrelo A, Vabres P, Diociaiuti A. Mosaic abnormalities of the skin: review and guidelines from the European Reference Network for rare skin diseases. Br J Dermatol. 2020; 182: 552–563. 4Cohen-Barak E, Mwassi B, Zagairy F, Danial-Farran N, Khayat M, Tatour Y, et al. Parental mosaic cutaneous-gonadal GJB2 mutation: from epidermal nevus to inherited ichthyosis-deafness syndrome. J Dermatol. 2022; 49: 379–382. 5Chassaing N, Kanitakis J, Sportich S, Cordier-Alex MP, Titeux M, Calvas P, et al. Generalized epidermolytic hyperkeratosis in two unrelated children from parents with localized linear form, and prenatal diagnosis. J Invest Dermatol. 2007; 126: 2715–2717. Early ViewOnline Version of Record before inclusion in an issue ReferencesRelatedInformation