Cargando…
ITGB4-mutated Junctional Epidermolysis Bullosa without Pyloric Atresia Presenting with Severe Urinary Involvement and Late-onset Minimal Skin Fragility: Diagnostic and Therapeutic Challenges
Autores principales: | MATTIOLI, Girolamo, DIOCIAIUTI, Andrea, ROSSI, Sabrina, ZAMBRUNO, Giovanna, CARLUCCI, Marcello, PISANESCHI, Elisa, EL HACHEM, May |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Publication of Acta Dermato-Venereologica
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631280/ https://www.ncbi.nlm.nih.gov/pubmed/35312019 http://dx.doi.org/10.2340/actadv.v102.935 |
Ejemplares similares
-
Case of Epidermolysis Bullosa with Pyloric Atresia
por: Kim, Jae-Hong, et al.
Publicado: (2011) -
Congenital Pyloric Atresia and Epidermolysis Bullosa: Report of a Rare Association
por: Pan, Pradyumna
Publicado: (2021) -
Case Report: Uncommon Association of ITGB4 and KRT10 Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis Congenita
por: Matyas, Melinda, et al.
Publicado: (2021) -
Plectin Deficiency Leads to Both Muscular Dystrophy and Pyloric Atresia in Epidermolysis Bullosa Simplex
por: Natsuga, Ken, et al.
Publicado: (2010) -
Case report: A case of epidermolysis bullosa complicated with pyloric atresia and a literature review
por: Luo, Caiyun, et al.
Publicado: (2023)