Abstract
Congenital chloride diarrhea (CCD) is a rare genetic disorder that causes persistent watery diarrhea, hyponatremia, hypochloremia, hypokalemia, severe metabolic alkalosis. Currently there are more than 250 described cases of this disease. The article summarizes international literature data on pathogenesis, clinical and symptomatic treatment of this disease, and presents its own clinical observations of a child with genetically confirmed CCD diagnosis.
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Artemova, I. V., Mitina, Y. Y., Britanishskaya, E. A., Shulakova, O. A., & Vaynshteyn, N. P. (2016). Congenital chloride diarrhea. Pediatriya - Zhurnal Im G.N. Speranskogo, 95(1), 137–139. https://doi.org/10.5468/kjog.2012.55.8.573
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