Congenital localized absence of skin (Bart syndrome) in a patient with dominant dystrophic epidermolysis bullosa
An Pediatr (Engl Ed)
.
2023 Dec;99(6):447-448.
doi: 10.1016/j.anpede.2023.04.016.
Epub 2023 Aug 17.
Authors
Francisco Javier Melgosa Ramos
1
,
Tania Díaz Corpas
2
,
Andrea Estébanez Corrales
2
,
Almudena Mateu Puchades
2
Affiliations
1
Servicio de Dermatología, Hospital Universitario Doctor Peset, Valencia, Spain. Electronic address: javimelgo2017@gmail.com.
2
Servicio de Dermatología, Hospital Universitario Doctor Peset, Valencia, Spain.
PMID:
37598075
DOI:
10.1016/j.anpede.2023.04.016
No abstract available
MeSH terms
Epidermolysis Bullosa Dystrophica* / complications
Epidermolysis Bullosa Dystrophica* / diagnosis
Epidermolysis Bullosa Dystrophica* / genetics
Humans
Skin
Syndrome