Case Report: Uncommon Association of ITGB4 and KRT10 Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis Congenita

Background: Epidermolysis bullosa is a rare form of genodermatosis produced by different gene mutations. The junctional form of the disease (JEB-PA) can associate pyloric atresia, renal abnormalities, and aplasia cutis congenita. Case Description: A case of a male preterm newborn with suspicion of d...

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Detalles Bibliográficos
Autores principales: Matyas, Melinda, Miclea, Diana, Zaharie, Gabriela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296908/
https://www.ncbi.nlm.nih.gov/pubmed/34306001
http://dx.doi.org/10.3389/fgene.2021.641977

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296908/
https://www.ncbi.nlm.nih.gov/pubmed/34306001
http://dx.doi.org/10.3389/fgene.2021.641977

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