186 top medical experts on congenital Sucrase-isomaltase deficiency across 12 countries and 18 U.S. states, including 26 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. congenital Sucrase-isomaltase deficiency: A rare, genetic, congenital carbohydrate intolerance disorder characterized by lack of endogenous sucrase activity, marked reduction in isomaltase activity, and moderate decrease in maltase activity, and clinically manifesting with diarrhea, abdominal pain and bloating, failure to thrive.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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  • Synonyms: Congenital Sucrase-Isomaltase Deficiency,  Congenital Sucrose Intolerance,  Congenital Sucrose-Isomaltose Malabsorption,  Congenital sucrose-isomaltase malabsorption,  Disaccharide Intolerance I,  1 Disaccharide intolerance,  Si Deficiency,  Sucrase-Isomaltase Deficiency,  Congenital Sucrose Intolerance,  Sucrose intolerance congenital,  Congenital Sucrose-Isomaltose Malabsorption,  congenital Sucrose-isomaltase malabsorption


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