Three successful pregnancies in a patient with glycogen storage disease type 0-Reference-Cited by-同舟云学术

Three successful pregnancies in a patient with glycogen storage disease type 0

Published:2020-10-26 Issue:1 Volume:57 Page:38-43
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Grünert Sarah C.¹^ORCID,Rosenbaum‐Fabian Stefanie¹,Hannibal Luciana¹,Schumann Anke¹,Spiekerkötter Ute¹

Affiliation:

1. Department of General Paediatrics, Adolescent Medicine and Neonatology Medical Centre‐University of Freiburg, Faculty of Medicine Freiburg Germany

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12178

Reference16 articles.

1. Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0.

2. Infantile Hypoglycaemia due to Inherited Deficiency of Glycogen Synthetase in Liver

3. A patient with glycogen storage disease type 0 and a novel sequence variant in GYS2: a case report and literature review;Arko JJ;J Int Med Res,2020

4. Hepatic glycogen synthase deficiency: An infrequently recognized cause of ketotic hypoglycemia

5. Glycogen storage diseases: Diagnosis, treatment and outcome

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