Novel Mutation of Gene Observed in Congenital Chloride Diarrhea
Congenital chloride diarrhea (CLD) is a rare autosomal recessive disease caused by mutations in the solute carrier family 26 member 3 (SLC26A3) gene on chromosome 7q31. Affected neonates are vulnerable to dehydration, electrolyte imbalance in the form of hyponatremia, metabolic alkalosis, failure to...
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| Main Authors: | , , |
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| Format: | Book |
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Korean Society of Neonatology,
2023-08-01T00:00:00Z.
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