Abstract
Congenital chloride diarrhoea (CCD) usually presents with abdominal distension, visible peristalsis and watery stools from birth that show chloride loss of more than 90 mmol/l. It may mimic low intestinal obstruction on antenatal ultrasound scanning after 30 weeks' gestation. This condition has been reported mainly from Finland. We report a case of CCD in a Saudi boy which was suspected antenatally, confirmed post-natally and managed successfully.
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CITATION STYLE
Abdullah, A. M. A., Shaheed, M. M., Katugampola, S. M., & Patel, P. J. (1990). Congenital chloride diarrhoea: Case report and review of the literature. Annals of Tropical Paediatrics, 10(1), 71–74. https://doi.org/10.1080/02724936.1990.11747412
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