Cori disease (with a Mnemonic) - Glycogen Storage Disease (Type III) - Learn about Glycogen Metabolism, Glycogen synthesis (Glycogenesis) and Glycogen breakdown (Glycogenolysis) - Metabolism - Clinical Biochemistry for doctors, nurses, pharmacists, physician assistants, dietitians, and premed students. | Medicosis Perfectionalis

Jordan has Glycogen Storage Disease Type 1a (GSD-1a) - which is a rare inherited metabolic disease that affects just 1 in 1.25 million people. It is caused by an #enzyme deficiency where the liver fails to break down glycogen into #glucose, causing the body’s blood sugar levels to drop. Moderna is committed to standing with the rare disease community to advance #mRNA research for patients living with #RareDiseases like GSD-1a. #RareDiseaseDay | Moderna, Inc.