Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
954 12 |
Ultima descărcare din IBN: 2021-04-05 18:35 |
Căutarea după subiecte similare conform CZU |
616.135-007-053.2-089 (1) |
Patologia sistemului circulator, a vaselor sanguine. Tulburări cardiovasculare (975) |
SM ISO690:2012 GAVRILIUC, Natalia, PALII, Ina, CIUBOTARU, Anatol, REPIN, Oleg, ZAHARIUC, Tatiana, CRIVCEANSCHI, Eugenia. Un caz rar de coarctaţie de aortă, complicată cu ruptură de anevrism gigantic la copil – raport de caz. In: Buletin de Perinatologie, 2017, nr. 3(75), pp. 66-69. ISSN 1810-5289. |
EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
Buletin de Perinatologie | ||||||
Numărul 3(75) / 2017 / ISSN 1810-5289 | ||||||
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CZU: 616.135-007-053.2-089 | ||||||
Pag. 66-69 | ||||||
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Descarcă PDF | ||||||
Rezumat | ||||||
Congenital aortophaties (CAo) occupies an important place in cardiovascular pathology in children. These pathologies include: aortic stenosis (AoSt), aortic coarctation (AoCo), bicuspid aortic valve (BAV), and aortic-related genetic diseases: Marfan syndrome (MS), Ehlers-Danlos syndrome. One of the most common is CoAo, which is a current medical problem with both high morbidity and severe complications that can develop instantly. It frequently develops asymptomatically and is a cause of complications such as aneurism, dilation, dissection, rupture, often fatal. These patients require regular assessments in specialized centers to avoid the onset of these complications and reduce the risk of sudden death |
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Cuvinte-cheie aortic coarctation, children., congenital aortopaties |
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Cerif XML Export
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These pathologies include: aortic stenosis (AoSt), aortic coarctation (AoCo), bicuspid aortic valve (BAV), and aortic-related genetic diseases: Marfan syndrome (MS), Ehlers-Danlos syndrome. One of the most common is CoAo, which is a current medical problem with both high morbidity and severe complications that can develop instantly. It frequently develops asymptomatically and is a cause of complications such as aneurism, dilation, dissection, rupture, often fatal. These patients require regular assessments in specialized centers to avoid the onset of these complications and reduce the risk of sudden death</p></cfAbstr> <cfAbstr cfLangCode='RU' cfTrans='o'><p>Врожденные аортопатии занимают важное место в сердечно-сосудистой патологии у детей. 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