Component of oligomeric Golgi complex 1 deficiency leads to hypoglycemia: a case report and literature review

Component of oligomeric Golgi complex 1 deficiency leads to hypoglycemia: a case report and literature review

Abstract Background Congenital disorders of glycosylation (CDG) are a group of metabolic diseases with clinical and genetic heterogeneity, and CDG-IIg is one of the rare reported types of CDG. The aim of this study is to report the clinical manifestations and gene-phenotype characteristics of a rare...

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Bibliographic Details
Main Authors: Yizhou Huang, Han Dai, Gangyi Yang, Lili Zhang, Shiyao Xue, Min Zhu
Format: Article
Language:English
Published: BMC 2021-10-01
Series:BMC Pediatrics
Subjects:
CDG-IIg
COG1 gene
case report
mutation
glycosylation
Online Access:https://doi.org/10.1186/s12887-021-02922-7

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