Estimating the proportions of allele frequencies for <i>SERPINA12</i> pathogenic variants in Japanese patients with Nagashima-type palmoplantar keratosis/keratoderma

Nagashima-type palmoplantar keratoderma (NPPK) is the most common form of palmoplantar keratoderma in Asian populations and is primarily caused by biallelic variants in SERPINB7. As SERPINA12 variants were reported in Chinese patients with NPPK, we analysed SERPINA12 variants in 18 Japanese patients with NPPK lacking biallelic SERPINB7 variants and found significantly higher frequencies of SERPINA12 variants c.635-7A&amp;gt;G and c.656A&amp;gt;G compared with the general population. This suggests a potential digenic effect involving SERPINB7 and SERPINA12, highlighting the need for considering digenic inheritance in NPPK diagnosis and genetic counselling.

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Publication Details

Journal
British Journal of Dermatology
Published
2025-03-26
DOI
https://doi.org/10.1093/bjd/ljaf111
Citations
2
Primary Topic
Skin and Cellular Biology Research
Type
article
Field-Weighted Citation Impact
2.30

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article

Estimating the proportions of allele frequencies for SERPINA12 pathogenic variants in Japanese patients with Nagashima-type palmoplantar keratosis/keratoderma

Basile Chrétien, Mariko Seishima, Yuika Suzuki, Yasushi Suga et al.
2 citations
British Journal of Dermatology
Skin and Cellular Biology Research
2.30
article

Estimating the proportions of allele frequencies for SERPINA12 pathogenic variants in Japanese patients with Nagashima-type palmoplantar keratosis/keratoderma

Basile Chrétien, Mariko Seishima, Yuika Suzuki, Yasushi Suga, Tomoo Ogi, Aoi Ebata, Ryo Fukaura, Kazuki Nishida, Takenori Yoshikawa, Akira Miyazaki, Takuya Takeichi, Yuka Nakazawa, Kana Tanahashi, Yoshinao Muro, Masashi Akiyama
article en
2 citations

Abstract

Nagashima-type palmoplantar keratoderma (NPPK) is the most common form of palmoplantar keratoderma in Asian populations and is primarily caused by biallelic variants in SERPINB7. As SERPINA12 variants were reported in Chinese patients with NPPK, we analysed SERPINA12 variants in 18 Japanese patients with NPPK lacking biallelic SERPINB7 variants and found significantly higher frequencies of SERPINA12 variants c.635-7A&amp;gt;G and c.656A&amp;gt;G compared with the general population. This suggests a potential digenic effect involving SERPINB7 and SERPINA12, highlighting the need for considering digenic inheritance in NPPK diagnosis and genetic counselling.

British Journal of DermatologyVol. 193(1)
Asahi University (JP), Nagoya University Hospital (JP), Juntendo University Urayasu Hospital (JP), Nagoya University (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 15%
Skin and Cellular Biology Research
2.30
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