English

Bart’s Syndrome: A Case Report

Bart's syndrome (BS) is a genetic disorder characterized by the absence of localized skin (present at birth), epidermolysis bullosa (EB) and ungueal changes [1]. Clinically Bart's syndrome is associated with epidermolysis bullosa (EB). It may be associated with any type of EB but is mostly reported with dominant dystrophic form. Diagnosis is obvious clinically but requires ultrastructural microscopy. Treatment suffices to conservative measures [1].

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