ABSTRACT

A series of hereditary illnesses known as epidermolysis bullosa (EB) are characterised by deteriorated dermo-epidermal integrity, blistering, and skin erosions caused by gene COL7A1 mutations. EBD-causing mutations can either be recessive or dominant. Mutations of type VII collagen, the main component of the anchoring fibrils, have been reported in recessive variants of epidermolysis bullosa dystrophica. mucous membranes following minor injury. In decreasing order of occurrence, EBD is distinguished by flat, pink, scar-producing bullae on the ankles, knees, hands, elbows, and feet. Only a few case reports of EBD have been documented in the literature. In this case report, the use of a symptoms healing treatment was evaluated in a 56 year old male patient. These disease relatively accounting as a rare disorders (incidence:1/50000 live births to 1/500000 live births).There is currently no effective treatment available; instead, operations are used to manage side effects and symptomatic relief. Keywords: Epidermolysis bullosa dystrophica, Skin lesion, Erosions, Hyperpigmentation, Dominant, Resessive
Publication date: 01/09/2023

https://ijbpas.com/pdf/2023/September/MS_IJBPAS_2023_7417.pdf

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https://doi.org/10.31032/IJBPAS/2023/12.9.7417