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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi Publishing Corporation
2016
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| Materias: | |
| 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 |