@article {Martinez‐Moreno:2020:0736-8046:821,
title = "Epidermolysis bullosa with congenital absence of skin: Review of the literature",
journal = "Pediatric Dermatology",
parent_itemid = "infobike://bsc/pde",
publishercode ="bp",
year = "2020",
volume = "37",
number = "5",
publication date ="2020-09-01T00:00:00",
pages = "821-826",
itemtype = "ARTICLE",
issn = "0736-8046",
eissn = "1525-1470",
url = "https://www.ingentaconnect.com/content/bsc/pde/2020/00000037/00000005/art00016",
doi = "doi:10.1111/pde.14245",
keyword = "aplasia cutis congenita, epidermolysis bullosa, Bart syndrome",
author = "MartinezMoreno, Adrian and OcampoCandiani, Jorge and AlbaRojas, Erika",
abstract = "Bart syndrome was initially described as association of congenital absence of skin (CAS), nail abnormalities, and epidermolysis bullosa (EB). Further reports of patients with CAS and EB have been made with wide clinical heterogeneity among them. Current guidelines recommend the elimination
of eponyms and use of the descriptive term EB with CAS.",
}