Mauriac syndrome (MS) is characterized by excessive intrahepatic glycogen deposition, attributed to severe hyperglycemia which diffuses by insulin-independent GLUT 2 to be trapped inside hepatocytes as G -6 phosphate. It can rarely occur in poorly controlled T1 diabetic adolescents and is complicated by hepatomegaly, short stature, delayed puberty and hypertriglyceridemia
(2024). Mauriac Syndrome; A Rare Complication of T1 DM. Egyptian Society of Diabetes and Lipidology Journal, 4(2), -. doi: 10.21608/esdlj.2024.456255
MLA
. "Mauriac Syndrome; A Rare Complication of T1 DM", Egyptian Society of Diabetes and Lipidology Journal, 4, 2, 2024, -. doi: 10.21608/esdlj.2024.456255
HARVARD
(2024). 'Mauriac Syndrome; A Rare Complication of T1 DM', Egyptian Society of Diabetes and Lipidology Journal, 4(2), pp. -. doi: 10.21608/esdlj.2024.456255
VANCOUVER
Mauriac Syndrome; A Rare Complication of T1 DM. Egyptian Society of Diabetes and Lipidology Journal, 2024; 4(2): -. doi: 10.21608/esdlj.2024.456255
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