A novel approach to characterize phenotypic variation in GSD IV: Reconceptualizing the clinical continuum
Purpose: Glycogen storage disease type IV (GSD IV) has historically been divided into discrete hepatic (classic hepatic, non-progressive hepatic) and neuromuscular (perinatal-congenital neuromuscular, juvenile neuromuscular) subtypes. However, the extent to which this subtype-based classification sy...
Main Authors: | Bridget T. Kiely, Rebecca L. Koch, Leticia Flores, Danielle Burner, Samantha Kaplan, Priya S. Kishnani |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-09-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2022.992406/full |
Similar Items
-
Two cases of a non-progressive hepatic form of glycogen storage disease type IV with atypical liver pathology
by: Keiko Ichimoto, et al.
Published: (2020-09-01) -
Induced pluripotent stem cell (iPSC) modeling validates reduced GBE1 enzyme activity due to a novel variant, p.Ile694Asn, found in a patient with suspected glycogen storage disease IV
by: Chie Naito, et al.
Published: (2024-06-01) -
An uncommon cause of early infantile liver disease and raised chitotriosidase
by: Srividya Sreekantam, et al.
Published: (2020-07-01) -
Case report: Familial glycogen storage disease type IV caused by novel compound heterozygous mutations in a glycogen branching enzyme 1 gene
by: Yiyang Li, et al.
Published: (2022-11-01) -
Biomarkers in Glycogen Storage Diseases: An Update
by: Alberto Molares-Vila, et al.
Published: (2021-04-01)