Mauriac syndrome is rare; we share our experience of nine patients who presented at a young age with malnutrition, short stature, abdominal distention and deranged liver function.
Otto-BuczkowskaEJaintaN. Mauriac syndrome — is already a history?Clin Diabetol2017; 6: 101–104.
2.
LombardoFPassanisiSGasbarroA, et al.Hepatomegaly and type 1 diabetes: a clinical case of Mauriac’s syndrome. Ital J Pediatr2019; 45: 3–3.
3.
FitzpatrickECotoiCQuagliaA, et al.Hepatopathy of Mauriac syndrome: a retrospective review from a tertiary liver centre. Arch Dis Child2014; 99: 354–357.
4.
MukewarSSharmaALackoreKA, et al.Clinical, biochemical, and histopathology features of patients with glycogenic hepatopathy. Clin Gastroenterol Hepatol2017; 15: 927–933.
5.
KhouryJZoharYShehadehN, et al.Glycogenic hepatopathy. Hepatobiliary Pancreat Dis Int2018; 17: 113–118.
6.
PandaPKSharawatIK. Mauriac syndrome in a young child with diabetes. Indian Pediatr2020; 57: 379–379.
7.
SantiETasciniGToniG, et al.Linear growth in children and adolescents with type 1 diabetes mellitus. Int J Environ Res Public Health2019; 16: 3677–3677.
8.
ParthasarathyLKhadilkarVChiplonkarS, et al.Longitudinal growth in children and adolescents with type 1 diabetes. Indian Pediatr2016; 53: 990–992.
9.
SherigarJMCastroJDYinYM, et al.Glycogenic hepatopathy: a narrative review. World J Hepatol2018; 10: 172–185.
10.
AydınFGerenliNDursunF, et al.Hepatopathies in children and adolescents with type 1 diabetes. J Pediatr Endocrinol Metab2019; 32: 121–126.