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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| Päätekijät: | , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2026-03-01
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| Sarja: | Frontiers in Pediatrics |
| Aiheet: | |
| Linkit: | https://www.frontiersin.org/articles/10.3389/fped.2026.1785578/full |
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