Please use this identifier to cite or link to this item: http://www.repositorio.uem.mz/handle258/1032
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dc.contributor.authorMocumbi, Ana O.-
dc.date.accessioned2024-06-11T07:55:44Z-
dc.date.available2024-06-11T07:55:44Z-
dc.date.issued2012-
dc.identifier.otherhttps://www.qscience.com/content/journals/10.5339/gcsp.2012.11-
dc.identifier.urihttp://www.repositorio.uem.mz/handle258/1032-
dc.description.abstractEndomyocardial fibrosis is a form of endemic restrictive cardiomyopathy that affects mainly childrenand adolescents, and is geographically restricted to some poor areas of Africa, Latin America andAsia. It is a condition with high morbidity and mortality, for which no effective therapy is available.Although several hypotheses have been proposed as triggers or causal factors for the disease, noneare able to explain the occurrence of the disease worldwide.In endemic areas of Africa endomyocardial fibrosis is as common a cause of heart failure asrheumatic heart disease, accounting for up to 20% of cases of heart failure and imposes aconsiderable burden to the communities and the health systems. However, due to lack of resourcesfor research in these areas, the exact epidemiology, etiology and pathogenesis remain unknown, andthe natural history is incompletely understood.We here review the main aspects of epidemiology, natural history, clinical picture and management ofendomyocardial fibrosis, proposing new ways to increase research into this challenging andneglected cardiovascular disease.en_US
dc.language.isoengen_US
dc.publisherGlobal Cardiology Science and Practiceen_US
dc.rightsopenAcessen_US
dc.subjectEndomyocardial fibrosisen_US
dc.subjectRestrictive cardiomyopathyen_US
dc.subjectEndemic diseaseen_US
dc.titleEndomyocardial fibrosis: a form ofendemic restrictive cardiomyopathen_US
dc.typearticleen_US
Appears in Collections:Artigos Publicados em Revistas Cientificas - FAMED

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