Prenatally suspected and clinically diagnosed congenital chloride diarrhea
Congenital chloride diarrhea (CCD) is a rare autosomal recessive disorder resulting from mutations in the SLC26A3 gene, leading to significant electrolyte imbalances and watery diarrhea starting in the prenatal period. Although prenatal diagnosis is ideal, many cases are identified postnatally. This...
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Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2025-03-01
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Series: | Radiology Case Reports |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S1930043324013876 |
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