Abstract
The Role of Genetic Mutation in Gene GBE1 In Induce Glycogen Storage Type IV Syndrome
Highlights
Glycogen type IV storage syndrome is a hereditary genetic disorder caused by excessive accumulation of glycogen sugar complexes in the body’s cells
The type of muscular nervous system is the most severe type of glycogen storage syndrome type IV, whose symptoms develop before birth and are usually fatal
It should be noted that most children with non-progressive liver glycogen storage syndrome reach puberty, life expectancy in these individuals varies depending on the severity of the symptoms and symptoms [4]
Summary
Glycogen type IV storage syndrome is a hereditary genetic disorder caused by excessive accumulation of glycogen sugar complexes in the body’s cells. This accumulated glycogen is structurally abnormal and disrupts the function of some organs, tissues, especially the liver and muscles. There are five types of type IV glycogen storage syndrome that have different signs and symptoms [1]
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