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Published in 2021 at "Baylor University Medical Center Proceedings"
DOI: 10.1080/08998280.2020.1866936
Abstract: Abstract Mauriac syndrome is an uncommon clinical condition arising in the setting of poorly controlled type 1 diabetes mellitus. Clinical features include hepatomegaly and liver abnormalities indistinguishable from nonalcoholic fatty liver disease. Early diagnosis and…
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Keywords:
persistent lactic;
mauriac syndrome;
type diabetes;
diabetes mellitus ... See more keywords
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1
Published in 2021 at "BMC Endocrine Disorders"
DOI: 10.1186/s12902-021-00835-1
Abstract: Background The Mauriac syndrome was described in 1930 as a peculiar combination of poorly controlled diabetes mellitus type 1, stunted growth and glycogenic hepatopathy. More recently, lactic acidosis was recognized as an additional feature, often…
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Keywords:
syndrome still;
lactate mauriac;
mauriac syndrome;
still mystery ... See more keywords
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Published in 2019 at "Journal of the Endocrine Society"
DOI: 10.1210/js.2019-mon-133
Abstract: Abstract Background: Glycogenic hepatopathy (GH: deposition of glycogen in the liver) and lactic acidosis (LA) in poorly controlled type 1 diabetes (T1D) can be the only presentation of Mauriac syndrome (hypercholesterolemia, growth retardation, delayed puberty,…
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Keywords:
dka;
lactate levels;
mauriac syndrome;
liver ... See more keywords
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Published in 2023 at "Revista espanola de enfermedades digestivas"
DOI: 10.17235/reed.2023.9513/2023
Abstract: The Pierre Mauriac syndrome described in the year 1930, is characterized by growth failure, cushingoid appearance, hepatomegaly and hypertransaminasemia, in a patient with chronic uncontrolled DM1. The most common age of presentation is usually in…
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Keywords:
syndrome importance;
mauriac syndrome;
syndrome;
hepatopathy mauriac ... See more keywords