Case Report: Two neonatal cases of genetically confirmed junctional epidermolysis bullosa in a tertiary care center

BackgroundEpidermolysis bullosa (EB) comprises a group of genetically heterogeneous disorders caused by defects in proteins responsible for dermoepidermal adhesion. Severe forms frequently present in the neonatal period and may be associated with early extracutaneous involvement, reflecting the wide...

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Autori principali:	Mohamad Hammoud, Soundos Youssef, Dana Maria Khoury, Malak Jbahi, Ali Dghaily, Salah Yamout, Rama Bdeir, Sara Mchad, Mazen Kurban, Samir Akel
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Frontiers Media S.A. 2026-03-01
Serie:	Frontiers in Pediatrics
Soggetti:	Carmi syndrome dystrophic EB EB-PA epidermolysis bullosa junctional Kindler epidermolysis bullosa
Accesso online:	https://www.frontiersin.org/articles/10.3389/fped.2026.1785578/full
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