Glycogen storage disease (GSD) IV is a rare autosomal recessive inherited disorder caused by mutations in the gene coding for glycogen branching enzyme leading to progressive liver disease. GSD IV is associated with mutations in , which encodes the glycogen branching enzyme. We report a case of GSD IV with rare homozygous mutations in the gene (c.791G>A (p.Gly264Glu), which was successfully treated by liver transplantation.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182483 | PMC |
http://dx.doi.org/10.5223/pghn.2018.21.4.365 | DOI Listing |
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