Thelansis

 Glycogen storage diseases (GSDs) are hereditary disorders resulting from inborn errors in carbohydrate metabolism. These disorders lead to abnormal glycogen storage and are categorized as GSDs. They are assigned numerical classifications based on identifying the enzyme defect responsible for the condition. Clinical symptoms can manifest from infancy to adulthood. GSDs can arise due to the accumulation of toxic glycogen and the inability to convert glycogen into energy. However, in all cases, they result in an inability to utilize or store glycogen. There are various types of glycogen storage diseases, with the following being the most prevalent: Glycogen storage disorders primarily affecting the liver encompass: ·        Glycogen synthase-2 deficiency (GSD type 0a) ·        Glucose-6-phosphatase deficiency (GSD type Ia) ·        Glucose-6-phosphate transporter deficiency (GSD type Ib)...