| Literature DB >> 32484238 |
Fuying Chen1,2, Linting Huang1,2, Changcan Li3, Jia Zhang1,2, Weiqin Yang1, Beibei Zhang1, Huaguo Li1,2, Dan Deng1,2, Jianying Liang1,2, Jinwen Shen1,2, Zhirong Yao1,2, Ming Li1,2.
Abstract
Epidermolysis bullosa (EB) is a heritable blistering disorder. We performed a next-generation sequencing-based multigene panel test and successfully predicted 100% of the EB types, including, 36 EB simplex (EBS), 13 junctional EB (JEB), 86 dystrophic EB (DEB), and 3 Kindler EB. Chinese JEB and recessive DEB (RDEB) patients have relatively mild phenotypes; for severe type separately accounts for 45.5% and 23.8%, respectively. We identified 96 novel and 49 recurrent pathogenic variants in 11 genes, although we failed to detect the second mutation in one JEB and five RDEB patients. We identified one novel p.E475K mosaic mutation in the clinically normal mother of one out of 13 EBS patients with KRT5 mutations, one recurrent p.G2034R mosaic mutation, and one novel p.G2043R mosaic mutation in the clinically normal relatives of two out of 19 dominant DEB patients. This study shows that next-generation technology could be an effective tool in diagnosing EB.Entities:
Keywords: epidermolysis bullosa; gene panel; genetic disease; pathogenic variant
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Year: 2020 PMID: 32484238 DOI: 10.1111/cge.13791
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438