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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

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