A case of Bart syndrome

Kankananarachchi, Imalke; Vithanage, Nimantha Dhananjaya; Munasinghe, Thilina Madushanka; Wanniarachchi, Charindu; Wijenayake, Binari K. S.; Jayantha, UK

doi:10.4038/sljch.v47i4.8605

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2020

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“…We reviewed the full text and references of 47 articles, and included 8 additional articles, for a total of 55 articles included in this review (Figure 1). 3,4,6‐58 Most were single or small case series of up to 6 patients, with an additional article by Chiaverini et al 39 reporting on 21 patients in whom gene testing was performed.…”

Section: Resultsmentioning

confidence: 99%

Epidermolysis bullosa with congenital absence of skin: Review of the literature

Martínez‐Moreno¹,

Ocampo‐Candiani²,

Alba‐Rojas³

2020

Pediatric Dermatology

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In 1966, Bart et al 1 described 20 members of a family with CAS affecting the lower extremities, blistering of the skin and mucous membranes, and nail abnormalities. This association of EB and CAS came to be known as Bart's syndrome (BS). At the time of the first report, the subtypes of EB were not classified because ultrastructural and immunochemical studies were not available. Years later, Zelickson et al 2 performed ultrastructural studies on the initial cases, demonstrating findings of dominant dystrophic epidermolysis

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Section: Resultsmentioning

confidence: 99%