Glycogen Storage Disease in Twins: When Two Lives Reflect One Silent Battle

Key Points

• The aim is to highlight the importance of early diagnosis and management of glycogen storage disease in infants.
• Identified symptoms such as hepatomegaly, hypoglycemia, and elevated liver enzymes in infants.
• Performed liver biopsy with PAS–diastase staining for definitive diagnosis.
• Implemented prompt metabolic management and regular follow-up care.
• Early recognition of symptoms leads to timely diagnosis.
• Metabolic management prevents progression to fibrosis.
• Long-term hepatic complications can be reduced with regular monitoring.