How do I know if I have Congenital Sucrase Isomaltase Deficiency?

What signs or symptoms may make you suspect you may have Congenital Sucrase Isomaltase Deficiency. People who have experience in Congenital Sucrase Isomaltase Deficiency offer advice of what things may make you suspicious and which doctor you should go to to receive treatment


Congenital Sucrase Isomaltase Deficiency (CSID) is a rare genetic disorder that affects the ability of the body to break down and absorb certain sugars, specifically sucrose and starches. This condition is present from birth and can lead to various digestive symptoms and nutritional deficiencies.



If you suspect you may have CSID, it is important to consult with a healthcare professional for a proper diagnosis. However, there are several signs and symptoms that may indicate the presence of this condition:



1. Digestive Symptoms: CSID often manifests with gastrointestinal issues such as chronic diarrhea, abdominal pain, bloating, and excessive gas. These symptoms may be present from infancy and can persist into adulthood.



2. Failure to Thrive: Infants with CSID may experience poor weight gain and growth due to the malabsorption of essential nutrients. This can be a significant concern and should be evaluated by a healthcare provider.



3. Developmental Delays: In some cases, CSID may be associated with delayed development, particularly in infants who experience severe malnutrition as a result of the condition. Early intervention and appropriate management are crucial to minimize potential developmental issues.



4. Dietary Intolerance: Individuals with CSID may have difficulty tolerating foods high in sucrose and starches. Consuming such foods can trigger digestive symptoms, leading to discomfort and malabsorption.



5. Family History: CSID is a genetic disorder, so having a family history of the condition increases the likelihood of being affected. If other family members have been diagnosed with CSID, it is important to discuss this with your healthcare provider.



If you experience any of these symptoms or suspect CSID, it is crucial to seek medical advice. A healthcare professional will perform various diagnostic tests, including genetic testing and breath tests, to confirm the presence of CSID. These tests can help differentiate CSID from other digestive disorders with similar symptoms.



Remember, only a qualified healthcare provider can provide an accurate diagnosis and appropriate treatment plan. If you suspect CSID or have concerns about your digestive health, make an appointment with a healthcare professional to discuss your symptoms and undergo the necessary tests.


by Diseasemaps

Ultimately a diagnosis can be made by a gastroenterologist. Initially visit your GP who can eliminate conditions like Coeliac. A food diary is very useful in the diagnosis, an 'elimination diet' may be necessary.

3/8/19 by Simone 3215

Stomach pains, severe bloating/wind or diarrhea. Need to see s gastroenterologist for diagnosis

11/15/21 by Tracey 3000

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