Grünert Sarah Catharina, Rosenbaum-Fabian Stefanie, Hannibal Luciana, Schumann Anke, Spiekerkoetter Ute
Department of General Paediatrics, Adolescent Medicine and Neonatology, Medical Centre- University of Freiburg, Faculty of Medicine, Mathildenstraße 1, 79106 Freiburg, Germany.
Mol Genet Metab Rep. 2021 May 8;27:100770. doi: 10.1016/j.ymgmr.2021.100770. eCollection 2021 Jun.
Glycogen storage disease type VI is caused by biallelic variants in the 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.
VI型糖原贮积病由导致肝糖原磷酸化酶缺乏的基因双等位基因变异引起。该疾病的临床特征为自婴儿期起出现肝肿大和反复酮症性低血糖。尽管大多数患者成年后无重大并发症,但迄今为止尚未有VI型糖原贮积病女性患者怀孕的报道。我们报告了一例VI型糖原贮积病患者成功妊娠并诞下健康后代的病例,并描述了产前和围产期管理情况。