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

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 case of...

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Detalles Bibliográficos
Autores principales: Huang, Yizhou, Dai, Han, Yang, Gangyi, Zhang, Lili, Xue, Shiyao, Zhu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8499485/
https://www.ncbi.nlm.nih.gov/pubmed/34625039
http://dx.doi.org/10.1186/s12887-021-02922-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8499485/
https://www.ncbi.nlm.nih.gov/pubmed/34625039
http://dx.doi.org/10.1186/s12887-021-02922-7

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