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1.
Plast Reconstr Surg Glob Open ; 8(3): e2666, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-32537331

RESUMO

Epidermolysis bullosa describes a rare group of genetic mucocutaneous disorders characterized by excessive epithelial fragility resulting in mechanically induced blistering and abnormal wound healing.1,2 Its prevalence and incidence are 8.2 and 19.6 per 1,000,000 live births, respectively.2 Gene therapy, protein replacement, and cell therapy strategies have been investigated, but there is currently no cure.2.

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