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- W2020545603 abstract "Objective To report a case of Mauriac syndrome in a young child with poorly controlled type 1 diabetes mellitus. Methods We describe the typical features of Mauriac syndrome and review the clinical, laboratory, and ultrasound findings and follow-up results in our current patient. Results Hepatomegaly, growth impairment, and cushingoid features characterize Mauriac syndrome. Most frequently, it is seen in adolescents and young adults with a history of poor glycemic control. In our current patient, a 3-year-old boy with type 1 diabetes mellitus of 2 years’ duration, Mauriac syndrome developed in the context of a disrupted social environment. His liver enzyme derangement, hepatomegaly, and growth improved once euglycemia was achieved. Conclusion Although Mauriac syndrome is currently uncommon, close monitoring of children with type 1 diabetes is important to maintain optimal glycemic control and prevent such an occurrence. (Endocr Pract. 2007;13: 63-66)" @default.
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- W2020545603 date "2007-01-01" @default.
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- W2020545603 title "Mauriac Syndrome in a 3-Year-Old Boy" @default.
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- W2020545603 doi "https://doi.org/10.4158/ep.13.1.63" @default.
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