Which are the causes of Congenital Sucrase Isomaltase Deficiency?

See some of the causes of Congenital Sucrase Isomaltase Deficiency according to people who have experience in Congenital Sucrase Isomaltase Deficiency


Congenital Sucrase Isomaltase Deficiency (CSID) is a rare genetic disorder that affects the digestive system. It is characterized by the body's inability to produce enough or any of the enzymes sucrase and isomaltase, which are essential for breaking down certain sugars and starches in the small intestine. This leads to difficulties in digesting and absorbing these carbohydrates, resulting in various gastrointestinal symptoms.



The causes of Congenital Sucrase Isomaltase Deficiency can be attributed to genetic mutations. The gene responsible for producing the sucrase-isomaltase enzyme is called SI, and mutations in this gene can lead to CSID. These mutations can be inherited from one or both parents, and the severity of the condition can vary depending on the specific genetic changes.



CSID is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to develop the disorder. If both parents carry a single copy of the mutated gene, they are considered carriers and have a 25% chance of having a child with CSID in each pregnancy.



While the exact prevalence of CSID is unknown, it is considered a rare disorder. It is more commonly diagnosed in infants and young children, as symptoms typically appear when solid foods are introduced into the diet. However, in some cases, CSID may not be diagnosed until later in childhood or even adulthood.



The symptoms of CSID can vary in severity and may include:




  • Chronic diarrhea

  • Abdominal pain and bloating

  • Excessive gas

  • Failure to thrive or poor weight gain

  • Vitamin and mineral deficiencies

  • Delayed growth and development



Diagnosis of CSID involves a combination of clinical evaluation, genetic testing, and specialized laboratory tests. A healthcare professional will assess the individual's symptoms, medical history, and family history to determine the likelihood of CSID. Genetic testing can confirm the presence of mutations in the SI gene, while specialized tests such as a sucrase activity test or a breath test can measure the individual's ability to digest certain sugars.



Management of CSID primarily involves dietary modifications. Individuals with CSID may need to follow a low-sugar or sugar-free diet, avoiding foods and beverages high in sucrose and starches that are difficult to digest. This may involve limiting the intake of certain fruits, vegetables, grains, and processed foods. In some cases, enzyme replacement therapy may be recommended to supplement the deficient enzymes and improve digestion.



With proper management and adherence to dietary recommendations, individuals with CSID can lead healthy lives. It is important for individuals with CSID and their families to work closely with healthcare professionals, such as dietitians and gastroenterologists, to ensure adequate nutrition and symptom control. Ongoing monitoring and follow-up are essential to address any potential complications and optimize overall health and well-being.


by Diseasemaps

I believe it is a genetic disorder. The terms GSID(Genetic Sucrase Isomaltase Deficiency) and CSID(Congenital Sucrase Isomaltase Deficiency) are interchangeable. The cause of the symptoms is a lack of the enzyme 'Sucrase' which breaks down the disaccharide 'Sucrose' into monosaccharides. Monosaccharides can be absorbed into the body in the intestine, disaccharides cannot. The undigested sugars(disaccharides) ferment in the intestine causing pain, gas, bloating leading to diarrhoea. Similarly a lack of the enzyme 'Isomaltase' which breaks down starch into smaller parts for absorption causes the same symptoms.

3/8/19 by Simone 3215

Emzyme deficiency, can be hereditary

11/15/21 by Tracey 3000

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