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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...
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| 出版年: | Case Rep Pediatr |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Hindawi Publishing Corporation
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5011225/ https://ncbi.nlm.nih.gov/pubmed/27635272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/2519498 |
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