| |
| | CSID Primer |
 | | Congenital Sucrase-isomaltase Deficiency (CSID) is a chronic malabsorption disease characterised by an autosomal recessive inheritable disease of sucrase and isomaltase deficiency (Hauri, 1985; Kerry, 1965; Naim, 1988; Newton, 1996). |
 | | Sucrase is an enzyme produced in the brush border lining of the small intestine and is responsible for the metabolism of sucrose, a disaccharide commonly known as table sugar, into two component monosaccharides, glucose and fructose, which are then absorbed into the circulation (Sterchi, 1990; Treem, 1995) |
 | | The absence of sucrase activity in patients as young as four months of age and symptoms in patients with CSID appearing as soon as sucrose is introduced to the diet, support the idea that this deficiency is present at birth. |
| sucraid.net /_wsn/page4.html (795 words) |
|