CONGENITAL CHLORIDE DIARRHEA: A CASE REPORT

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NIK AVAR A.

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Journal: Iranian Journal of Pediatrics Year:2007 | Volume:17 | Issue:2 Page(s): 179-182

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Title

CONGENITAL CHLORIDE DIARRHEA: A CASE REPORT

Author(s)

NIK AVAR A. | Issue Writer Certificate

Keywords

CONGENITAL CHLORIDE DIARRHEAQ3

METABOLIC ALKALOSISQ3

HYPOKALEMIAQ3

HYPOCHLOREMIAQ3

HYPERURICOSURIAQ3

Abstract

Objective: CONGENITAL CHLORIDE DIARRHEA (CCD) is a rare autosomal recessive disorder of intestinal chloride absorption. Pathognomonic features consist of watery diarrhea, failure to thrive, dehydration and hypokalemic hypochloremic METABOLIC ALKALOSIS.Case Presentation: This is the report on an 8-month old Iranian girl with severe and complicated course of CCD and poor response to current treatment. In addition, she had a renal tubular defect in uric acid handling, resulted in persistent HYPERURICOSURIA and hypouricemia.Conclusion: Specific characteristics of CCD in our population need additional investigation. But, it is recommended to consider CCD in any patient with severe resistant diarrhea to prevent its irreversible and long term organ damage.

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APA: Copy

NIK AVAR, A.. (2007). CONGENITAL CHLORIDE DIARRHEA: A CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS, 17(2), 179-182. SID. https://sid.ir/paper/76221/en

Vancouver: Copy

NIK AVAR A.. CONGENITAL CHLORIDE DIARRHEA: A CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2007;17(2):179-182. Available from: https://sid.ir/paper/76221/en

IEEE: Copy

A. NIK AVAR, “CONGENITAL CHLORIDE DIARRHEA: A CASE REPORT,” IRANIAN JOURNAL OF PEDIATRICS, vol. 17, no. 2, pp. 179–182, 2007, [Online]. Available: https://sid.ir/paper/76221/en

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