A glycogen storage disease type 1a patient with type 2 diabetes

A glycogen storage disease type 1a patient with type 2 diabetes

Abstract Background Glycogen storage disease type 1a (GSD1a) is an inborn genetic disease caused by glucose-6-phosphatase-α (G6Pase-α) deficiency and is often observed to lead to endogenous glucose production disorders manifesting as hypoglycemia, hyperuricemia, hyperlipidemia, lactic acidemia, hepa...

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Bibliographic Details
Main Authors: Yi Sun, Wenhui Qiang, Runze Wu, Tong Yin, Jie Yuan, Jin Yuan, Yunjuan Gu
Format: Article
Language:English
Published: BMC 2022-09-01
Series:BMC Medical Genomics
Subjects:
GSD1a
T2DM
G6PC gene
Online Access:https://doi.org/10.1186/s12920-022-01344-3

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