Mauriac syndrome — is already a history?

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Mauriac syndrome still exists.

BACKGROUND/OBJECTIVE Mauriac syndrome (MS) is a rare complication of type 1 diabetes mellitus (DM1). It is related to low insulin concentrations and is less common since longer-acting insulins became available. It is characterized by hepatomegaly, growth and puberty delay, and the presence of elevated transaminases and serum lipids. The aim of this study was to describe the patients from a pedi...

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Mauriac syndrome and early cataract diabetic

Result A 5 year and 10 month old boy, was admitted with protuberant abdomen since one year ago. He had been recognized as type 1 DM and treated by subcutaneous insulin 4-5 U/day twice a day until admission. His abdomen became larger, wasted arms and legs so he couldn’t support his body, and just laid down for 3 months. He had retarded growth and development. Oedema face, chest was normal, diste...

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Face processing in Williams syndrome is already atypical in infancy

Face processing is a crucial socio-cognitive ability. Is it acquired progressively or does it constitute an innately-specified, face-processing module? The latter would be supported if some individuals with seriously impaired intelligence nonetheless showed intact face-processing abilities. Some theorists claim that Williams syndrome (WS) provides such evidence since, despite IQs in the 50s, ad...

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Hepatic glycogenosis in type 1 diabetes mellitus mimicking Mauriac syndrome

Hepatic glycogenosis in type 1 diabetes mellitus (DM) can be caused by poor glycemic control due to insulin deficiency, excessive insulin treatment for diabetic ketoacidosis, or excessive glucose administration to control hypoglycemia. Mauriac syndrome, which is characterized by hepatomegaly due to hepatic glycogenosis, growth retardation, delayed puberty, and Cushingoid features, is a rare dia...

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ژورنال

عنوان ژورنال: Clinical Diabetology

سال: 2017

ISSN: 2450-8187,2450-7458

DOI: 10.5603/dk.2017.0016