McArdle disease, also known as glycogen storage disease type V, is an inherited metabolic disorder marked by a deficiency of myophosphorylase, the enzyme essential for the breakdown of glycogen in ...

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 ...

Unexplained left ventricular hypertrophy often prompts the diagnosis of hypertrophic cardiomyopathy, a sarcomere-protein gene disorder. Because mutations in the gene for AMP-activated protein kinase γ ...

Glycogen storage disorders are inborn errors of metabolism that typically affect the cellular architecture and function of the liver or kidney. However, some of these diseases manifest in skeletal or ...

DUBLIN--(BUSINESS WIRE)--The "Glycogen Storage Disorders (GSD) Ongoing Global Clinical Trials Analysis and Outlook" report has been added to ResearchAndMarkets.com's offering. Glycogen Storage ...

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 ...