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Published on: August 20, 2019
A heterozygous mutation in ITGB4 causing a mild phenotype of junctional epidermolysis bullosa
Zhongtao Li1,2, Lin Wang1,2, Sheng Wang1,2
1Department of Dermatology, West China Hospital, Sichuan University, Chengdu, China.
Abstract:
Mutations in ITGB4 are known to cause autosomal recessive junctional epidermolysis bullosa (JEB), which is manifested by severe blistering and granulation tissue, usually complicating pyloric atresia and even leading to death. ITGB4-associated autosomal dominant epidermolysis bullosa has rarely been documented. Herein, we identified a heterozygous pathogenic variant (c.433G>T; p.Asp145Tyr) in ITGB4 causing a mild phenotype of JEB in a Chinese family.
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