Novel Mutations in PSENEN Gene in Two Chinese Acne Inversa Families Manifested as Familial Multiple Comedones and Dowling-Degos Disease

作者：Zhou, Cheng; Wen, Guang-Dong; Soe, Lwin Myint; Xu, Hong-Jun; Du, Juan; Zhang, Jian-Zhong^*

来源：Chinese Medical Journal, 2016, 129(23): 2834-2839.

DOI：10.4103/0366-6999.194648

• Acne Inversa
• Comedones
• Dowling-Degos Disease
• Hidradenitis Suppurativa
• PSENEN
• Squamous Cell Carcinoma

Background: Acne inversa (AI), also called hidradenitis suppurativa, is a chronic, inflammatory, recurrent skin disease of the hair follicle. Familial AI shows autosomal-dominant inheritance caused by mutations in the gamma-secretase genes. This study was aimed to identify the specific mutations in the gamma-secretase genes in two Chinese families with AI. @@@ Methods: In this study, two Chinese families with AI were investigated. All the affected individuals in the two families mainly manifested with multiple comedones, pitted scars, and a few inflammatory nodules on their face, neck, trunk, axilla, buttocks, upper arms, and thighs. Reticulate pigmentation in the flexures areas resembled Dowling-Degos disease clinically and pathologically. In addition, one of the affected individuals developed anal canal squamous cell carcinoma. Molecular mutation analysis of gamma-secretase genes including PSENEN, PSEN1, and NCSTN was performed by polymerase chain reaction and direct DNA sequencing. @@@ Results: Two novel mutations of PSENEN gene were identified, including a heterozygous missense mutation c. 194T>G (p.L65R) and a splice site mutation c. 167-2A>G. @@@ Conclusions: The identification of the two mutations could expand the spectrum of mutations in the gamma-secretase genes underlying AI and provide valuable information for further study of genotype-phenotype correlations.

• 出版日期2016-12-5
• 单位北京大学