Congenital Chloride Diarrhea: Diagnosis by Easy-Accessible Chloride Measurement in Feces

Background. Congenital chloride diarrhea (CCD) is an autosomal recessive disorder caused by mutations in the genes encoding the intestinal Cl(−)/HCO(3) (−) exchanger and is clinically characterized by watery, profound diarrhea, electrolyte disturbances, and metabolic alkalosis. The CCD diagnosis is...

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Detalles Bibliográficos
Autores principales: Gils, C., Eckhardt, M.-C., Nielsen, P. E., Nybo, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011225/
https://www.ncbi.nlm.nih.gov/pubmed/27635272
http://dx.doi.org/10.1155/2016/2519498

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011225/
https://www.ncbi.nlm.nih.gov/pubmed/27635272
http://dx.doi.org/10.1155/2016/2519498

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