Retrospective analysis of clinical characteristics and outcomes in 132 patients with hepatic glycogen storage diseases, highlighting unique complications.
Key Points
Most patients presented with distinct symptoms like abdominal distention and hypoglycemia.
A significant 84.9% showed hepatomegaly and 20.5% demonstrated splenomegaly, crucial for diagnosis.
Non-hepatic malignancies and structural anomalies were notably observed, highlighting unusual complications.
The study emphasizes the importance of genetic analysis for accurate diagnosis and management of hepatic glycogenosis.