Dual clinical features of fine and rough scales seen in a combined ichthyosis vulgaris and X-linked recessive ichthyosis patient with atopic dermatitis

The Journal of DermatologyEarly View LETTER TO THE EDITOR Dual clinical features of fine and rough scales seen in a combined ichthyosis vulgaris and X-linked recessive ichthyosis patient with atopic dermatitis Yoshimasa Nakane, Yoshimasa Nakane orcid.org/0000-0002-6428-9814 Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, JapanSearch for more papers by this authorTakenori Yoshikawa, Takenori Yoshikawa Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, JapanSearch for more papers by this authorTakuya Takeichi, Corresponding Author Takuya Takeichi [email protected] orcid.org/0000-0001-5958-2875 Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan Correspondence Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan. Email: [email protected] and [email protected]Search for more papers by this authorMichihiro Kono, Michihiro Kono Department of Dermatology and Plastic Surgery, Akita University Graduate School of Medicine, Akita, JapanSearch for more papers by this authorMasashi Akiyama, Corresponding Author Masashi Akiyama [email protected] orcid.org/0000-0001-5863-9315 Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan Correspondence Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan. Email: [email protected] and [email protected]Search for more papers by this author Yoshimasa Nakane, Yoshimasa Nakane orcid.org/0000-0002-6428-9814 Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, JapanSearch for more papers by this authorTakenori Yoshikawa, Takenori Yoshikawa Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, JapanSearch for more papers by this authorTakuya Takeichi, Corresponding Author Takuya Takeichi [email protected] orcid.org/0000-0001-5958-2875 Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan Correspondence Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan. Email: [email protected] and [email protected]Search for more papers by this authorMichihiro Kono, Michihiro Kono Department of Dermatology and Plastic Surgery, Akita University Graduate School of Medicine, Akita, JapanSearch for more papers by this authorMasashi Akiyama, Corresponding Author Masashi Akiyama [email protected] orcid.org/0000-0001-5863-9315 Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan Correspondence Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan. Email: [email protected] and [email protected]Search for more papers by this author First published: 21 September 2023 https://doi.org/10.1111/1346-8138.16968Read 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 1Nomura T, Sandilands A, Akiyama M, Liao H, Evans AT, Sakai K, et al. Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis. J Allergy Clin Immunol. 2007; 119: 434–440. 2Hand JL, Runke CK, Hodge JC. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray. J Am Acad Dermatol. 2015; 72: 617–627. 3Süßmuth K, Gruber R, Rodriguez E, Traupe H, Amler S, Sánchez-Guijo A, et al. Increased prevalence of filaggrin deficiency in 51 patients with recessive X-linked ichthyosis presenting for dermatological examination. J Invest Dermatol. 2018; 138: 709–711. 4Ramesh R, Chen H, Kukula A, Wakeling EL, Rustin MH, McLean WH. Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations. J Dermatol Sci. 2011; 64: 159–162. 5Zhang Q, Si N, Liu Y, Zhang D, Wang R, Zhang Y, et al. Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome. Gene. 2017; 628: 103–108. Early ViewOnline Version of Record before inclusion in an issue ReferencesRelatedInformation