Bart syndrome: A case report of neonatal disorder.
aplasia cutis
ectodermal dysplasia
epidermolysis bullosa
infant
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Feb 2024
Feb 2024
Historique:
received:
27
11
2023
revised:
20
01
2024
accepted:
04
02
2024
medline:
12
2
2024
pubmed:
12
2
2024
entrez:
12
2
2024
Statut:
epublish
Résumé
Bart Syndrome, characterized by congenital skin absence, blistering, and nail abnormalities, presents complex neonatal challenges. This rare condition demands a multidisciplinary approach for accurate diagnosis and comprehensive care.
Identifiants
pubmed: 38344349
doi: 10.1002/ccr3.8528
pii: CCR38528
pmc: PMC10857911
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e8528Informations de copyright
© 2024 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
The authors declare no conflicts of interest related to the research presented in this article. There are no financial or personal relationships with individuals or organizations that could inappropriately influence or bias the content and findings of this work.
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