Division of Dermatology, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Pediatr Dermatol. 2020 Sep;37(5):955-957. doi: 10.1111/pde.14239. Epub 2020 Jun 16.
Bullous dermolysis of the newborn is a subtype of dystrophic epidermolysis bullosa that typically resolves within the first two years of life. We present a case of autosomal dominant bullous dermolysis of the newborn and report a novel pathogenic mutation. This case highlights that collagen VII mutations may present clinically with a mild phenotype.
新生儿大疱性表皮松解症是营养不良性大疱性表皮松解症的一个亚型,通常在生命的头两年内自行消退。我们报告了一例常染色体显性遗传的新生儿大疱性表皮松解症,并报道了一个新的致病突变。本病例提示 VII 型胶原基因突变可表现出临床表型较轻。