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Images in Paediatrics
Congenital localized absence of skin (Bart syndrome) in a patient with dominant dystrophic epidermolysis bullosa
Ausencia congénita de piel (síndrome de Bart) en un paciente con epidermólisis ampollosa distrófica dominante
Francisco Javier Melgosa Ramos
Corresponding author
javimelgo2017@gmail.com

Corresponding author.
, Tania Díaz Corpas, Andrea Estébanez Corrales, Almudena Mateu Puchades
Servicio de Dermatología, Hospital Universitario Doctor Peset, Valencia, Spain
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Article information
ISSN: 23412879
Original language: English
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Anales de Pediatría (English Edition)
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