Glycogen Storage Disease Type IX due to a Novel Mutation in PHKA2 Gene

<div>(a) Hemotoxylin and eosin (H&amp;E) stain showing enlarged and distended hepatocytes with clear cytoplasm. (b) Periodic acid-Schiff (PAS) stain showing increased glycogen content in the cytoplasm of hepatocytes. (c) Periodic acid-Schiff-diastase (PAS-D) stain showing the removal of glycogen from hepatocytes with the diastase staining.</div>

Case Reports in Pediatrics

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Figure 1

Figure 1: Glycogen Storage Disease Type IX due to a Novel Mutation in PHKA2 Gene 