Sucrase isomaltase deficiency

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congenital sucrose isomaltose malabsorption

Facts (generated by robot; please edit if you find it inaccurate)

  • Congenital sucrase-isomaltase deficiency is an example of a disease in which mutant phenotypes generate transport-incompetent molecules.
  • Sucrase-isomaltase deficiency is a rare disorder usually manifested as diarrhea in infancy.
  • Alternative Names Given to the Disorder Congenital Sucrase-Isomaltase Deficiency is also known as Disaccharide Intolerance I, SI Deficiency, Congenital Sucrose Intolerance and CSID.
  • Sucrase-isomaltase deficiency is much rarer and is also genetically heterogeneous.
  • (Lon)aSucrase-isomaltase deficiency is a rare disorder usually manifested as diarrhea in infancy.

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