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: Qian Li, Jing Wang, Ruixian Zang, Lichun Yu, Zhenle Yang and Shuzhen Sun Tags: Case Report Source Type: research