Glycogen storage diseases (GSDs) constitute a group of inherited metabolic disorders that impair normal glycogen synthesis or degradation, resulting in the accumulation of structurally abnormal ...

Estimates suggest that glycogen storage diseases (GSD) affect from around one person in 40,000 to less than one person in 1,000,000, making them “ultra-rare” diseases. This results in diluted research ...

Pompe disease also known as Glycogen Storage Disease / Acid Maltase Deficiency is a rare genetic disease caused by the buildup of a sugar called glycogen in the body’s cells. It is caused by the ...

Dublin, Nov. 18, 2024 (GLOBE NEWSWIRE) -- The "Glycogen Storage Disorders (GSD): Competitive Landscape" report has been added to ResearchAndMarkets.com's offering. This reports provides a data-driven ...

At Week 96 participants experienced even greater reductions in daily cornstarch intake while maintaining low levels of hypoglycemia, improved levels of euglycemia and improved fasting tolerance Phase ...

A team of Canadian and Japanese researchers has identified the genetic mutation responsible for glycogen storage disease type IIIa in Inuit in northern Quebec, Canada, in a study published in CMAJ ...