Congenital chloride diarrhoea in a Chinese infant with a compound heterozygous SLC26A3 mutation

Congenital chloride diarrhoea (CCD) is an autosomal recessive condition that causes secretory diarrhoea and potentially deadly electrolyte imbalances in infants because of solute carrier family 26 member 3 (SLC26...
Source: BMC Pediatrics - Category: Pediatrics Authors: Tags: Case Report Source Type: research