Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
907 7 |
Ultima descărcare din IBN: 2017-05-07 16:27 |
Căutarea după subiecte similare conform CZU |
575.1:616.127-053.2 (1) |
General genetics. General cytogenetics (427) |
Pathology of the circulatory system, blood vessels. Cardiovascular complaints (975) |
SM ISO690:2012 STAMATI, Adela. Genetic issues in pediatric hypertrophic
cardiomyophaty. In: Buletinul Academiei de Ştiinţe a Moldovei. Ştiinţele vieţii, 2015, nr. 2(326), pp. 47-52. ISSN 1857-064X. |
EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
Buletinul Academiei de Ştiinţe a Moldovei. Ştiinţele vieţii | ||||||
Numărul 2(326) / 2015 / ISSN 1857-064X | ||||||
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CZU: 575.1:616.127-053.2 | ||||||
Pag. 47-52 | ||||||
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Rezumat | ||||||
Hypertrophic cardiomyopathy (HCM) is a common genetic cardiovascular disease. It is marked by phenotypic and genotypic heterogeneity. A retrospective study was performed on 23 children with HCM, aged before 19 years, hospitalized in Department of Pediatric cardiology of Child and Mother Institute (2008-2012). All subjects underwent detailed assessment: clinical history and examination, 12-lead and Holter monitoring electrocardiogram (ECG) and transthoracic echocardiographic study. Each clinical case was analyzed with reference to detection the presence of unfavorable risk factors. We are guided by the recommendations of pediatric studies, including extracardiac involving. According to clinical data, 3 infant was suspected for mitochondrial disease. The multidisciplinary approach has a considerable advantage in everyday assessment of children with HCM. 28 references, 4 tables. |
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Cuvinte-cheie genetic, pediatric hypertrophic cardiomyopathy |
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