What is it about?
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].
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Why is it important?
Bart syndrome is a rare neonatal pathology combining congenital skin aplasia affecting the extremities and exceptionally described congenital epidermolysis bullosa [2].
Perspectives
Bart syndrome is a rare neonatal pathology combining congenital skin aplasia affecting the extremities and exceptionally described congenital epidermolysis bullosa [2].
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This page is a summary of: Bart’s Syndrome: A Case Report, Journal of Case Reports and Medical History, October 2022, Acquire Publications LLC,
DOI: 10.54289/jcrmh2200131.
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