一名 LAMC2 基因突变杂合子婴儿的表皮松解症:病例报告

Q4 Medicine
G. Milas, Vasiliki Tsolaki, Vasileios Issaris, Stefanos Fragkos, Aakash Pandita
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引用次数: 0

摘要

大疱性表皮松解症是由与皮肤完整性和真皮-表皮粘连相关的基因引起的一种异质性皮肤病。主要分为四大类:单纯性表皮松解症、交界性表皮松解症、萎缩性表皮松解症和金勒综合征。我们报告了一例一个月大的婴儿因发烧和大疱性表皮松解症而被送到急诊科的病例。皮肤培养对甲氧西林敏感的金黄色葡萄球菌和大肠杆菌呈阳性。全外显子组测序发现LAMC2基因发生了突变。交界性表皮松解症与预后不良有关。医护人员和家长应接受专门的教育,因为这种疾病的患者需要特殊护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidermolysis Bullosa in an Infant Heterozygous for Mutation in LAMC2 Gene: A Case Report
Epidermolysis bullosa is a heterogenous skin disease caused by genes associated with skin integrity and dermal–epidermal adhesion. The four main categories include: epidermolysis bullosa simplex, junctional epidermolysis bullosa, dystrophic epidermolysis bullosa, and kindler syndrome. We report the case of a one-month-old infant who was brought to the emergency department due to complaint of fever and a bullous exanthem. Skin cultures were positive for methicillin-sensitive Staphylococcus aureus and Escherichia coli. Whole exome sequencing revealed mutations in LAMC2 gene. Junctional epidermolysis bullosa is associated with poor prognosis. Healthcare professionals and parents should be educated in a specific way as patients with this condition are in need of special care.
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来源期刊
Journal of Neonatology
Journal of Neonatology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
55
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