Mucosal Abnormalities in Children With Congenital Chloride Diarrhea—An Underestimated Phenotypic Feature?

Objectives and Study: Congenital chloride diarrhea (CCD) is a rare, autosomal recessive disorder caused by mutations in the SLC26A3 gene encoding a transmembrane chloride/bicarbonate ion exchanger mainly expressed in the apical brush border of the ileal and colonic epithelium. Lifelong, secretory, c...

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Detalles Bibliográficos
Autores principales: Kurteva, Elena, Lindley, Keith J., Hill, Susan M., Köglmeier, Jutta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403178/
https://www.ncbi.nlm.nih.gov/pubmed/32850522
http://dx.doi.org/10.3389/fped.2020.00365

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403178/
https://www.ncbi.nlm.nih.gov/pubmed/32850522
http://dx.doi.org/10.3389/fped.2020.00365

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