Congenital form of glycogen storage disease type IV: A case report and a review of the literature
- 1 August 2004
- journal article
- case report
- Published by Wiley in Pediatrics International
- Vol. 46 (4), 474-477
- https://doi.org/10.1111/j.1442-200x.2004.01916.x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
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- Intravenous immune globulin in lysinuric protein intoleranceJournal of Inherited Metabolic Disease, 1998
- Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.JCI Insight, 1996
- Neonatal hypotonia and cardiomyopathy secondary to type?IV glycogenosisActa Neuropathologica, 1994
- A Congenital Variant of Glycogenosis Type IVFetal and Pediatric Pathology, 1993
- Fetal Storage DisordersPublished by Springer Science and Business Media LLC ,1990
- Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotesJournal of Inherited Metabolic Disease, 1988
- Glycogenosis IV: A new cause of infantile hypotoniaThe Journal of Pediatrics, 1972