A Novel Nonsense Mutation of the ATP2C1 Gene in an 18-Year-Old-Female with Papular Acantholytic Dyskeratosis of the Anogenital Area

Papular acantholytic dyskeratosis (PAD), often found to occur in the vulvar or anogenital area, is an exceedingly rare skin condition that usually presents in adulthood and features multiple smooth skin-colored or grayish-white papules with or without pruritus. Although the pathogenesis of PAD is unknown, PAD may be associated with mutations in ATP2C1 and ATP2A2 genes. Here, we report on an 18-year-old female patient with multiple gray-white flat papules in the anogenital area. Skin biopsy revealed hyperkeratosis of the epidermis, acantholysis, formation of fissures or lacunae, and disappearance of desmosomes. Whole exon sequencing (WES) of the patient indicated mutations in the ATP2C1 gene.

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Publication Details

Journal
Clinical Cosmetic and Investigational Dermatology
Published
2024-12-01
DOI
https://doi.org/10.2147/ccid.s498588
Citations
1
Primary Topic
Skin and Cellular Biology Research
Type
article
Field-Weighted Citation Impact
0.33
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article

A Novel Nonsense Mutation of the ATP2C1 Gene in an 18-Year-Old-Female with Papular Acantholytic Dyskeratosis of the Anogenital Area

Nai-Chao Feng, Chuan Wan, Moath alhadidi, Shuqi Huang
1 citations
Clinical Cosmetic and Investigational Dermatology
Skin and Cellular Biology Research
0.33
article

A Novel Nonsense Mutation of the ATP2C1 Gene in an 18-Year-Old-Female with Papular Acantholytic Dyskeratosis of the Anogenital Area

Nai-Chao Feng, Chuan Wan, Moath alhadidi, Shuqi Huang
article en
1 citations

Abstract

Papular acantholytic dyskeratosis (PAD), often found to occur in the vulvar or anogenital area, is an exceedingly rare skin condition that usually presents in adulthood and features multiple smooth skin-colored or grayish-white papules with or without pruritus. Although the pathogenesis of PAD is unknown, PAD may be associated with mutations in ATP2C1 and ATP2A2 genes. Here, we report on an 18-year-old female patient with multiple gray-white flat papules in the anogenital area. Skin biopsy revealed hyperkeratosis of the epidermis, acantholysis, formation of fissures or lacunae, and disappearance of desmosomes. Whole exon sequencing (WES) of the patient indicated mutations in the ATP2C1 gene.

Clinical Cosmetic and Investigational DermatologyVol. Volume 17
Nanchang University (CN)
Gender equality
Openalex Percentile: Top 39%
Skin and Cellular Biology Research
0.33
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