scholarly journals A Rare Case of Left Ventricular Noncompaction in LEOPARD Syndrome

2018 ◽  
Vol 26 (1) ◽  
pp. 43
Author(s):  
Kyehwan Kim ◽  
Min Gyu Kang ◽  
Hyun Woong Park ◽  
Jin-Sin Koh ◽  
Jeong Rang Park ◽  
...  
2010 ◽  
Vol 90 (6) ◽  
pp. 2047-2049 ◽  
Author(s):  
Kirill O. Barbukhatty ◽  
Sergey Y. Boldyrev ◽  
Olga A. Rossokha ◽  
Elena D. Kosmacheva ◽  
Vladimir A. Porhanov

2016 ◽  
Vol 2016 ◽  
pp. 1-5 ◽  
Author(s):  
Karan Wats ◽  
On Chen ◽  
Nupur Nippun Uppal ◽  
Syeda Atiqa Batul ◽  
Norbert Moskovits ◽  
...  

Left ventricular noncompaction cardiomyopathy is a rare myocardial disorder which results from failure of left ventricle to compact in embryogenesis. We present a case of a 53-year-old female who came because of abdominal pain and was found to have renal infarct secondary to noncompaction cardiomyopathy.


2018 ◽  
Vol 27 (3) ◽  
pp. 208-209
Author(s):  
Christos Tourmousoglou ◽  
Harilaos Bogossian ◽  
Vlasis Ninios ◽  
Elias Ninios

Ebstein’s anomaly is a rare congenital cardiac disease characterized by apical displacement of the tricuspid valve with decreased right ventricular function. Left ventricular noncompaction is a cardiomyopathy characterized by the presence of numerous and prominent trabeculations together with deep intertrabecular recesses in a portion of the ventricular wall, principally at the lateral and apical level. We describe the very rare case of a patient living for 78 years with a benign form of Ebstein’s anomaly and left ventricular noncompaction cardiomyopathy with slightly reduced systolic function.


2018 ◽  
Vol 69 (8) ◽  
pp. 2209-2212
Author(s):  
Alexandru Radu Mihailovici ◽  
Vlad Padureanu ◽  
Carmen Valeria Albu ◽  
Venera Cristina Dinescu ◽  
Mihai Cristian Pirlog ◽  
...  

Left ventricular noncompaction is a primary cardiomyopathy with genetic transmission in the vast majority of autosomal dominant cases. It is characterized by the presence of excessive myocardial trabecularities that generally affect the left ventricle. In diagnosing this condition, echocardiography is the gold standard, although this method involves an increased risk of overdiagnosis and underdiagnosis. There are also uncertain cases where echocardiography is inconclusive, a multimodal approach is needed, correlating echocardiographic results with those obtained by magnetic resonance imaging. The clinical picture may range from asymptomatic patients to patients with heart failure, supraventricular or ventricular arrhythmias, thromboembolic events and even sudden cardiac death. There is no specific treatment of left ventricular noncompaction, but the treatment is aimed at preventing and treating the complications of the disease. We will present the case of a young patient with left ventricular noncompactioncardiomyopathy and highlight the essential role of transthoracic echocardiography in diagnosing this rare heart disease.


2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Patrizia Saccucci ◽  
Federica Papetti ◽  
Roberta Martinoli ◽  
Alessandro Dofcaci ◽  
Ursula Tuderti ◽  
...  

A 16-year-old boy affected by Sotos syndrome was referred to our clinic for cardiac evaluation in order to play noncompetitive sport. Physical examination was negative for major cardiac abnormalities and rest electrocardiogram detected only minor repolarization anomalies. Transthoracic echocardiography showed left ventricular wall thickening and apical trabeculations with deep intertrabecular recesses, fulfilling criteria for isolated left ventricular noncompaction (ILVNC). Some sporadic forms of ILVNC are reported to be caused by a mutation on CSX gene, mapping on chromosome 5q35. To our knowledge, this is the first report of a patient affected simultaneously by Sotos syndrome and ILVNC.


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