To understand the genetic characteristics and clinical features of Kindler Syndrome in the Chinese population, this study included data from OMIM (https://www.omim.org/), Wan Fang (https://www.wanfangdata.com.cn/index.html), CNKI (https://c61.oversea.cnki.net/), and PubMed (https://pubmed.ncbi.nlm.nih.gov/) databases to conduct a literature review on the clinical phenotypes and genetic backgrounds of FERMT1 variant patients in China (Table 1). This evidence concerns the gene FERMT1 and Kindler syndrome.