Cardiovascular Malformations
Mostrando 1-12 de 34 artigos, teses e dissertações.
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1. Coarctation of The Aorta: A Case-Series from a Tertiary Care Hospital
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 2020-02
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2. Coarctation of the Aorta: Its Importance for Pediatricians and Cardiologists
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 2020-02
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3. Coarctation of The Aorta: A Case-Series from a Tertiary Care Hospital
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 08/08/2019
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4. Risk factors and comorbidities in Brazilian patients with orofacial clefts
Abstract: Considering that environmental risk factors substantially contribute to the etiology of orofacial clefts and that knowledge about the characteristics and comorbidities associated with oral clefts is fundamental to promoting better quality of life, this study aimed to describe the risk factors, main characteristics, and comorbidities of a group of p
Braz. oral res.. Publicado em: 05/04/2018
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5. Detecção da microdeleção 7q11.23 por MLPA® e estudo clínico dos pacientes com síndrome de Williams-Beuren / Detection of the microdeletion 7q11.23 by MLPA® and clinical study of patients with Williams-Beuren syndrome
INTRODUCTION: Williams-Beuren syndrome (WBS) is a genetic disorder caused by a microdeletion in 7q11.23 region. It is characterized by typical facial dysmorphisms, mental retardation, hipersociable behavior, congenital heart disease, mainly supravalvular aortic stenosis (SVAS), and other variable congenital malformations. METHODS: 65 patients (40 males, 25 f
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 30/05/2012
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6. Síndrome de deleção 22q11.2 e cardiopatias congênitas
OBJETIVO: Revisar as características clínicas, etiológicas e diagnósticas da síndrome de deleção 22q11 e sua associação com as cardiopatias congênitas. FONTES DOS DADOS: Foram pesquisados artigos científicos presentes nos portais Medline, Lilacs e SciELO, utilizando-se descritores específicos como "22q11", "DiGeorge syndrome", "velocardiofacial s
Revista Paulista de Pediatria. Publicado em: 2011-06
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7. Importance and repercussions of renal and cardiovascular pathology on stroke in young adults: an anatomopathologic study of 52 clinical necropsies
INTRODUCTION: Stroke in young adults has seldom been studied in a necropsy series. The objective of the present clinical necropsy-based investigation was to analyze stroke and its relationship with cardiovascular and renal pathology in young adults. MATERIALS AND METHODS:The protocols of 52 clinical necropsies with diagnoses of stroke in patients aged 18 - 4
Clinics. Publicado em: 2008
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8. Relationship between the maternal diabetes and the sexual development of the male rat offspring / Relação entre o diabete materno e o desenvolvimento sexual da prole masculina de ratos
Diabetes melllitus is a group of metabolic disorders of multiple etiology, characterized by defects in the secretion and/or action of insulin. The causes of the disease can be genetic and/or environmental. Diabetes is one of the most common metabolic complications during pregnancy and is associated with an increased risk of maternal and neonatal morbidities.
Publicado em: 2007
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9. MalformaÃÃo arteriovenosa cerebral: estudo da angioarquitetura em indivÃduos da regiÃo nordeste do Brasil
As MalformaÃÃes Arteriovenosas Cerebrais (MAVs) sÃo lesÃes vasculares provocadas pela persistÃncia de fÃstulas arteriovenosas primitivas, apresentam aspecto em novelo com pedÃculos arteriais e veias de drenagem hipertrofiadas. As MAVs podem provocar hemorragias, sendo os riscos de hemorragias intracranianas de aproximadamente 50%; destes, 30% chegam a
Publicado em: 2005
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10. Desempenho do ultra-som pre-natal como metodo para diagnostico de cromossomopatias fetais
The objective of this study was to determine the performance of ultrasound in detecting risk pregnancies as to fetal cytogenetical abnormality. A group of 454 patients was retrospectively studied. They underwent ultra-sound and fetal karyotype over the last five years. A total of 291 women presented abnormal ultrasound and 163 presented normal ultrasound. Ul
Publicado em: 1998
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11. Prevalence of cardiovascular malformations and association with karyotypes in Turner's syndrome.
The aim of the study was to establish the prevalence of cardiovascular malformations in females with Turner's syndrome and analyse possible associations with the various karyotypes. One hundred and seventy nine of 393 females who had Turner's syndrome diagnosed in Denmark were examined. Complete chromosome analysis was available in all cases. Clinical examin
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12. Cardiovascular malformation in infant deaths. 10-year clinical and epidemiological study.
The infant mortality from cardiovascular malformations in a region with a population of 2 million inhabitants during a 10-year period has been studied. The study involved validation of the diagnoses and judgement whether the cardiovascular malformation was the dominating or a contributing cause of death. It is shown that the incidence of fatal cardiovascular