Familial benign chronic pemphigus or Hailey-Hailey disease (OMIM 169600) is an autosomal-dominant blistering disease. Here we present a rare case of familial benign chronic pemphigus in a Chinese infant. The 5-month-old proband, who showed diffusely distributed skin lesions, is the youngest patient of Hailey-Hailey disease ever reported. The detection of an ATP2C1 gene mutation in this infant confirmed the diagnosis. His mother carried the same mutation, but with no history of skin lesions.
基金：
Beijing Natural Science FoundationBeijing Natural Science Foundation [7062023, 7092031]
第一作者机构：[1]Capital Med Univ, Beijing Childrens Hosp, Dept Dermatol, Beijing 100045, Peoples R China;
通讯作者：
通讯机构：[1]Capital Med Univ, Beijing Childrens Hosp, Dept Dermatol, Beijing 100045, Peoples R China;[3]Capital Med Univ, Beijing Childrens Hosp, Dept Dermatol, 56 Nan Lishi Rd, Beijing 100045, Peoples R China
推荐引用方式(GB/T 7714)：
Xu Zhe,Zhang Lixin,Xiao Yuanyuan,et al.A Case of Hailey-Hailey Disease in an Infant with a New ATP2C1 Gene Mutation[J].PEDIATRIC DERMATOLOGY.2011,28(2):165-168.doi:10.1111/j.1525-1470.2010.01088.x.
APA：
Xu, Zhe,Zhang, Lixin,Xiao, Yuanyuan,Li, Li,Lin, Zhimiao...&Ma, Lin.(2011).A Case of Hailey-Hailey Disease in an Infant with a New ATP2C1 Gene Mutation.PEDIATRIC DERMATOLOGY,28,(2)
MLA：
Xu, Zhe,et al."A Case of Hailey-Hailey Disease in an Infant with a New ATP2C1 Gene Mutation".PEDIATRIC DERMATOLOGY 28..2(2011):165-168
