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Bookmark or Share- Glycogen Storage Disease (GSD) - Cleveland ClinicGSD type I (von Gierke disease), the most common type, occurs in approximately 1 in 100,000 births. What are the symptoms of glycogen storage disease? The symptoms of glycogen storage disease can vary based on the type and even from person to person with the same type.
- Glycogen Storage Disease Type I - Symptoms, Causes, Treatment | NORDGlycogen storage disease type I (GSDI) is characterized by accumulation of excessive glycogen and fat in the liver and kidneys that can result in an enlarged liver and kidneys and growth retardation leading to short stature.
- Glycogen Storage Disease - StatPearls - NCBI BookshelfA short duration of fasting that results in typical symptoms suggests glycogen storage disorder type I or III. If an overnight duration of fasting leads to hypoglycemic symptoms, then glycogen storage disease type 0, VI, or IX should be considered. Laboratory Testing. Hypoglycemia should be documented by measuring serum glucose levels.
- Glycogen storage disease type I - WikipediaGlycogen storage disease type I (GSD I) is an inherited disease that prevents the liver from properly breaking down stored glycogen, which is necessary to maintain adequate blood sugar levels. GSD I is divided into two main types, GSD Ia and GSD Ib, which differ in cause, presentation, and treatment.
- Glycogen Storage Disease Type I - GeneReviews® - NCBI BookshelfGlycogen storage disease type I (GSD I) is characterized by accumulation of glycogen and fat in the liver and kidneys resulting in hepatomegaly and nephromegaly. Severely affected infants present in the neonatal period with severe hypoglycemia due to fasting intolerance.
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