Glycogen storage disease: Revision history

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16 November 2022

  • curprev 15:2815:28, 16 November 2022‎ Aidan talk contribs‎ 4,775 bytes +4,775‎ Created page with "{| class="wikitable" !Class !Defect !Clinical Clues !Diagnosis !Therapy |- |GSD 0a |Glycogen synthase 2 deficiency in liver | * Ketotic hypoglycemia * No hepatomegaly | * Liver biopsy and enzyme testing * DNA testing | * Uncooked cornstarch * Commercial glucose polymers (eg, Glycosade) * Liver transplantation |- |GSD 0b |muscle glycogen synthase deficiency | * Cardiomyopathy * Exercise intolerance * Weakness | * Muscle biopsy (glycogen depletion) * Enzyme assay * DNA tes..." Tag: Visual edit
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