Congenital Sucrase-Isomaltase Deficiency (CSID)
CSID is a rare inherited metabolic disorder characterized by the deficiency or absence of the enzymes sucrase and isomaltase. When the concentration of this enzyme complex is low or absent, the breakdown of the disaccharide sucrose and starch and the subsequent absorption of smaller molecular components cannot take place.
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To schedule an appointment, please call the office of Singaram Gastroenterology at 605-310-2000.