Congenital Sucrase Isomaltase Deficiency Synonyms
Congenital Sucrase Isomaltase Deficiency (CSID) is a rare genetic disorder that affects the digestive system. It is also known by several other names, including:
- Sucrase-Isomaltase Deficiency: This term refers to the lack or deficiency of the enzymes sucrase and isomaltase, which are responsible for breaking down sugars in the small intestine.
- Genetic Sucrase-Isomaltase Deficiency: This name highlights the genetic nature of the disorder, indicating that it is present from birth and is inherited.
- Isomaltase Deficiency: This term specifically focuses on the deficiency of the enzyme isomaltase, which plays a crucial role in digesting certain carbohydrates.
- Disaccharidase Deficiency: CSID falls under the category of disaccharidase deficiencies, which are characterized by the body's inability to break down certain types of sugars.
- Carbohydrate Malabsorption: CSID can also be referred to as carbohydrate malabsorption, as it involves the impaired absorption of specific carbohydrates due to the enzyme deficiency.
These synonyms are often used interchangeably to describe the same condition, highlighting the various aspects of the disorder's underlying mechanisms and symptoms. It is important to note that while the names may differ, they all refer to the same genetic disorder that affects the digestion of sugars in the small intestine.