Successful pregnancy in a woman with glycogen storage disease type 6
2021
Sarah Catharina Grünert | Stefanie Rosenbaum-Fabian | Luciana Hannibal | Anke Schumann | Ute Spiekerkoetter
Glycogen storage disease type VI is caused by biallelic variants in the PYGL gene that result in hepatic glycogen phosphorylase deficiency. The disorder is clinically characterized by hepatomegaly and recurrent ketotic hypoglycemia from infancy. Although most patients reach adulthood without major complications, no pregnancies in women with GSD VI have been reported so far. We report on a successful pregnancy in a GSD VI patient that resulted in a healthy offspring and describe the pre- and perinatal management.
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