scholarly journals Presentación de un caso de síndrome de Mauriac

2017 ◽  
Vol 3 (3) ◽  
pp. 26-32
Author(s):  
Yessica Agudelo Zapata ◽  
Camilo Andrés Quintero Cadavid ◽  
Héctor Fabio Sandoval Alzate ◽  
Luis Miguel Maldonado ◽  
Roberto Franco Vega

Se presenta un paciente con diabetes mellitus tipo 1, con una complicación poco frecuente conocida como síndrome de Mauriac. Se realizan ayudas diagnósticas tendientes a descartar diagnósticos diferenciales como la mucopolisacaridosis tipo I, que se consideró una de las enfermedades de depósito más probables en el caso del paciente. Finalmente, se presenta una discusión del caso, resumiendo los aspectos fundamentales que llevaron a la sospecha del síndrome de Mauriac. Abstract This is a case report of a patient with diabetes mellitus type 1 and a rare complication known as Mauriac syndrome. Laboratory tests were performed to rule out differential diagnoses, such as mucopolysaccharidosis type I, which was considered one of the storage diseases, most likely for the patient. Finally, we present a discussion of the case, summarizing the key issues that led to the suspicion of a Mauriac syndrome.

2017 ◽  
Vol 34 (4) ◽  
pp. 132-134 ◽  
Author(s):  
Umang G Thakkar ◽  
Aruna V Vanikar ◽  
Hargovind L Trivedi

2022 ◽  
Vol 18 ◽  
Author(s):  
Spyridon Maragkoudakis ◽  
Vasiliki Katsi ◽  
Andreas Melidonis ◽  
Stergios Soulaidopoulos ◽  
Genovefa D. Kolovou ◽  
...  

Abstract: Diabetes mellitus type 1 (T1DM) is an autoimmune disease characterized by a markedly elevated cardiovascular (CV) risk due to premature atherosclerosis. Previous studies have shown that intense glycemic control reduces the incidence of CV disease. Antiplatelet therapy is considered to be a very important therapy for secondary prevention of recurrent atherothrombotic events in patients with DM, while it may be considered for primary prevention in individuals with T1DM with additional CV risk factors.The aim of the present review is to summarize existing literature data regarding the thrombotic risk in T1DM patients and discuss current treatment strategies.


2018 ◽  
Vol 5 (12) ◽  
pp. 1
Author(s):  
Maria João Rodrigues Ferreira Pinto ◽  
Nuno Melo ◽  
Luís Flores ◽  
Francisco Cunha

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
P. Mukhopadhyay ◽  
R. Barai ◽  
C. A. Philips ◽  
J. Ghosh ◽  
S. Saha

Diabetic Myonecrosis is a rare complication of long-standing Diabetes Mellitus Type 1 and 2. The most likely affected areas are of proximal lower limbs, mostly the quadriceps muscle. The presenting features are myriad and a diagnostic conundrum for the physician. There has been previously mentioned, through few case reports, the classical presentation of diabetes-related muscle infarction. Here we present a patient of diabetic myonecrosis, in whom the initial presentation of diabetes mellitus was that of bilateral symmetric proximal upper limb predominant muscle infarction, which has never been reported before.


Author(s):  
Julia Marian ◽  
Firdous Rizvi ◽  
Lily Q. Lew

AbstractNonketotic hyperglycemic chorea-ballism (NKHCB), also known as diabetic striato-pathy (DS) by some, is a rare complication of diabetes mellitus and uncommon in children. We report a case of a 10 11/12-year-old boy of Asian descent with uncontrolled type 1 diabetes mellitus (T1DM), Hashimoto's thyroiditis, and multiple food allergies presenting with bilateral chorea-ballism. His brain magnetic resonance imaging revealed developmental venous anomaly in right parietal lobe and right cerebellum, no focal lesions or abnormal enhancements. Choreiform movements resolved with correction of hyperglycemia. Children and adolescents with a movement disorder should be evaluated for diabetes mellitus, especially with increasing prevalence and insidious nature of T2DM associated with obesity.


2015 ◽  
Author(s):  
Anzhalika Solntsava ◽  
Olga Zagrebaeva ◽  
Nadeya Peskavaya ◽  
Viktoryia Kozel ◽  
Hanna Mikhno

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