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ReserarchID
DV75O
Left ventricular noncompaction is a rare cause of cardiomyopathy, sometimes with a family character that may complicate evolving with heart failure, heart rhythm disorders and systemic embolic events -including stroke. We report a case of a young patient in neurological dispensary for epilepsy where the neuroimaging evaluation of an acutely installed cephalalgia syndrome revealed multiple silent lacunar brain injuries. Paraclinical examinations of their etiology have led to the diagnosis of a left ventricular noncompaction, in this context the lacunar infarcts beeing considered as cerebral embolic events with a cardiac starting point.
Mihaela Lungu. 2018. \u201cSilent Lacunary Brain Infarctions Associated with Left Ventricular Noncompaction and Idiopathic Epilepsy A Case Report\u201d. Global Journal of Medical Research - K: Interdisciplinary GJMR-K Volume 18 (GJMR Volume 18 Issue K4): .
Crossref Journal DOI 10.17406/gjmra
Print ISSN 0975-5888
e-ISSN 2249-4618
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Total Score: 104
Country: Romania
Subject: Global Journal of Medical Research - K: Interdisciplinary
Authors: Mihaela Lungu, Violeta Sapira, Doina Carina Voinescu, Manuela Arbune (PhD/Dr. count: 0)
View Count (all-time): 124
Total Views (Real + Logic): 3084
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Publish Date: 2018 07, Tue
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Left ventricular noncompaction is a rare cause of cardiomyopathy, sometimes with a family character that may complicate evolving with heart failure, heart rhythm disorders and systemic embolic events -including stroke. We report a case of a young patient in neurological dispensary for epilepsy where the neuroimaging evaluation of an acutely installed cephalalgia syndrome revealed multiple silent lacunar brain injuries. Paraclinical examinations of their etiology have led to the diagnosis of a left ventricular noncompaction, in this context the lacunar infarcts beeing considered as cerebral embolic events with a cardiac starting point.
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