Expanding the SLURP1 disease spectrum: from Mal de Meleda to palmoplantar keratoderma/progressive symmetric erythrokeratoderma

Takuya Takeichi^{1

2}, Chao-Kai Hsu^{3

4

5}

Affiliations

¹ Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
² Nagoya University Institute for Advanced Research, Nagoya, Japan.
³ Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
⁴ Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
⁵ International Center of Wound Repair and Regeneration, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

Editorial

Takuya Takeichi et al. Br J Dermatol. 2025.

. 2025 Apr 28;192(5):793.

doi: 10.1093/bjd/ljaf059.

Takuya Takeichi^{1

2}, Chao-Kai Hsu^{3

4

5}

¹ Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
² Nagoya University Institute for Advanced Research, Nagoya, Japan.
³ Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
⁴ Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
⁵ International Center of Wound Repair and Regeneration, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

No abstract available

Conflict of interest statement

Conflicts of interest: The authors declare no conflicts of interest.

Autosomal dominant SLURP1 variants cause palmoplantar keratoderma and progressive symmetric erythrokeratoderma.
Jiang X, Mortlock RD, Lomakin IB, Zhou J, Hu R, Cossio ML, Bunick CG, Choate KA. Jiang X, et al. Br J Dermatol. 2025 Apr 28;192(5):896-906. doi: 10.1093/bjd/ljaf049. Br J Dermatol. 2025. PMID: 39913669