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Ultrastructure and molecular pathogenesis of epidermolysis bullosa.

机译:大疱表皮松解的超微结构和分子发病机制。

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摘要

Epidermolysis bullosa (EB) is classified into the three major subtypes depending on the level of skin cleavage within the epidermal keratinocyte or basement membrane zone. Tissue separation occurs within the intraepidermal cytoplasm of the basal keratinocyte, through the lamina lucida, or in sublamina densa regions of the basal lamina (basement membrane) in EB simplex, junctional EB, and dystrophic EB, respectively. Transmission electron microscopy (TEM) is an effective method for determining the level of tissue separation and hemidesmosome (HD) and anchoring fibril morphology if performed by experienced operators, and has proven to be a powerful technique for the diagnosis of new EB patients. Recent advances in genetic and immunofluorescence studies have enabled us to diagnose EB more easily and with greater accuracy. This contribution reviews TEM findings in the EB subtypes and discusses the importance of observations in the molecular morphology of HD and basement membrane associated structures.
机译:大疱表皮松解症(EB)根据表皮角质形成细胞或基底膜区域内的皮肤裂解水平分为三种主要亚型。组织分离发生在基底角质形成细胞的表皮内细胞质中,通过透明层,或分别在单纯EB,交界性EB和营养不良性EB的基底层的基底膜下层(基底膜)中。透射电子显微镜(TEM)是由经验丰富的操作员执行的用于确定组织分离和半桥粒(HD)和锚定纤维形态的有效方法,并且已被证明是诊断新EB患者的有力技术。遗传和免疫荧光研究的最新进展使我们能够更轻松,更准确地诊断EB。该贡献回顾了EB亚型中的TEM发现,并讨论了观察在HD和基底膜相关结构的分子形态中的重要性。

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