scholarly journals Mauriac Syndrome: A Rare Complication of Type 1 Diabetes Mellitus

2018 ◽  
Vol 5 (12) ◽  
pp. 1
Author(s):  
Maria João Rodrigues Ferreira Pinto ◽  
Nuno Melo ◽  
Luís Flores ◽  
Francisco Cunha
2017 ◽  
Vol 34 (4) ◽  
pp. 132-134 ◽  
Author(s):  
Umang G Thakkar ◽  
Aruna V Vanikar ◽  
Hargovind L Trivedi

Author(s):  
Abinash Subedi ◽  
Vishnu Charan Suresh Kumar ◽  
Anuj Sharma ◽  
Gilles Hoilat ◽  
Savio John

QJM ◽  
2020 ◽  
Vol 113 (Supplement_1) ◽  
Author(s):  
M H Elsayed ◽  
M T Hamza ◽  
M M Elsaeed ◽  
R A F Thabet

Abstract Glycogenic hepatopathy (GH) is a very rare complication seen mostly in patients with type 1 diabetes mellitus (T1DM) in whom glycemic control has been poor for a long time. We assessed liver diseases in children and adolescents with type 1 diabetes mellitus by detection of elevated liver transaminases and confirmed by fibro scan and ultrasound. One hundred and seven children and adolescents with T1DM were subjected to detailed history, physical examination, laboratory investigation and radiological investigation. Liver transaminases, mean HbA1c and pelviabdominal ultrasound were done for all patients while fibro scan for those with elevated liver enzymes only. Patients with elevated liver enzymes were reassessed after one year. Only nine of our patients have elevated liver enzymes. HbA1c and fibro scan abnormalities (F stage) were significantly higher in patients with elevated liver enzymes. (p < 0.001) After follow up a significant decrease in liver enzymes, fibro scan abnormalities and HbA1c in the group with elevated liver enzymes initially was detected. (p < 0.001) We concluded that liver disease is not a common complication in patients with long standing uncontrolled diabetes which can be reversed after proper control.


2011 ◽  
Vol 14 (3) ◽  
pp. 116-119
Author(s):  
Natalya Alexandrovna Molitvoslovova ◽  
Alla Yur'evna Tokmakova

We describe the case of Mauriac syndrome in young adult with prolonged poorly controlled type 1 diabetes mellitus.


2011 ◽  
Vol 2011 (jul19 1) ◽  
pp. bcr0320113975-bcr0320113975 ◽  
Author(s):  
M. S. Shrivastava ◽  
A. V. Palkar ◽  
N. J. Padwal ◽  
N. Moulick

2019 ◽  
Vol 32 (12) ◽  
pp. 1391-1394
Author(s):  
Junichi Suzuki ◽  
Tatsuo Fuchigami ◽  
Kengo Kawamura ◽  
Masako Aoki ◽  
Tatsuhiko Urakami ◽  
...  

Abstract Background Diabetic ketoacidosis (DKA) is a common complication of type 1 diabetes mellitus (T1DM). Infants and children with new-onset T1DM may present with DKA, and the risk of cerebral edema is high in infantile DKA. What is new? Neurological deterioration during an episode of DKA is usually attributed to cerebral edema and cerebrovascular accidents. However, cerebral infarction is a very rare complication in infantile DKA. Case presentation We describe a rare case of infantile cerebral infarction caused by severe DKA in a patient with new-onset T1DM. Conclusions Cerebral infarction is an important intracranial complication in infantile DKA. Careful observation and treatment for DKA during the first 24 h of therapy are necessary in infants with new-onset T1DM because the risk of cerebral infarction is highest during this timeframe.


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