What does congenital disorder of glycosylation mean?
Definitions for congenital disorder of glycosylation
con·gen·i·tal dis·or·der of gly·co·sy·la·tion
This dictionary definitions page includes all the possible meanings, example usage and translations of the word congenital disorder of glycosylation.
Wikipedia
Congenital disorder of glycosylation
A congenital disorder of glycosylation (previously called carbohydrate-deficient glycoprotein syndrome) is one of several rare inborn errors of metabolism in which glycosylation of a variety of tissue proteins and/or lipids is deficient or defective. Congenital disorders of glycosylation are sometimes known as CDG syndromes. They often cause serious, sometimes fatal, malfunction of several different organ systems (especially the nervous system, muscles, and intestines) in affected infants. The most common sub-type is PMM2-CDG (formally known as CDG-Ia) where the genetic defect leads to the loss of phosphomannomutase 2 (PMM2), the enzyme responsible for the conversion of mannose-6-phosphate into mannose-1-phosphate.
Numerology
Chaldean Numerology
The numerical value of congenital disorder of glycosylation in Chaldean Numerology is: 5
Pythagorean Numerology
The numerical value of congenital disorder of glycosylation in Pythagorean Numerology is: 3
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"congenital disorder of glycosylation." Definitions.net. STANDS4 LLC, 2024. Web. 28 Apr. 2024. <https://www.definitions.net/definition/congenital+disorder+of+glycosylation>.
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