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Modified 'Stent-Graft Sandwich' Technique for Treatment of Isolated Common Iliac Artery Aneurysm in Patient With Marfan Syndrome
(Elsevier B.V., 2012-04-01)
Isolated iliac artery aneurysms are rare in the general population (0.03%) and represent 2% of all abdominal aneurysms, and the association with Marfan syndrome is even rarer. We report a Marfan syndrome case with an ...
Modified 'Stent-Graft Sandwich' Technique for Treatment of Isolated Common Iliac Artery Aneurysm in Patient With Marfan Syndrome
(Elsevier B.V., 2012-04-01)
Isolated iliac artery aneurysms are rare in the general population (0.03%) and represent 2% of all abdominal aneurysms, and the association with Marfan syndrome is even rarer. We report a Marfan syndrome case with an ...
Immediate effects of submaximal effort on pulse wave velocity in patients with Marfan syndrome
(Associação Brasileira de Divulgação Científica, 2010-04-01)
Marfan syndrome (MS) is a dominant autosomal disease caused by mutations in chromosome 15, the locus controlling fibrillin 1 synthesis, and may exhibit skeletal, ocular, cardiovascular, and other manifestations. Pulse wave ...
Modelling and numerical simulation of the in vivo mechanical response of the ascending aortic aneurysm in marfan syndrome
Marfan syndrome (MFS) is a genetic disorder that affects connective tissue, impairing cardiovascular structures and function, such as heart valves and aorta. Thus, patients with Marfan disease have a higher risk of developing ...
Descripción de la calidad de vida y evaluación del nivel de conocimiento de un individuo con síndrome de Marfan sobre su enfermedad y el tipo de mutación que se presenta a nivel molecular
(Ediciones Universidad Simón BolívarFacultad de Ciencias de la Salud, 2019)
El síndrome de Marfan (SMF) es una enfermedad del sistema conectivo de tipo autosómica
dominante de afección multiorgánica. Su buen pronóstico dependerá de un eficiente
diagnóstico, tratamiento y al acoplamiento del ...
Pectus excavatum como debut de Síndrome de Marfan. Reporte de caso
(2020)
Introduction: Marfan syndrome (MS) is an autosomal dominant disorder characterized by connective tissue disorders; in which tall stature, elongated limbs and fingers are associated with ...
Hypermobility and Ehlers-Danlos syndromes: Clinical aspects and patient's quality of life
(Centro de Estudios Académicos en Neuropsicología, 2016)
There is an urgent need to increase the Joint Hypermobility Syndrome (JHS) awareness, that for most authors is the same as the Ehlers-Danlos Hypermobility type (formerly called EDS type III) that is a congenital, very ...
Syndromic and non-syndromic aneurysms of the human ascending aorta share activation of the Smad2 pathway
(JOHN WILEY & SONS LTD, 2009)
Common features such as elastic fibre destruction, mucoid accumulation, and smooth muscle cell apoptosis are co-localized in aneurysms of the ascending aorta of various aetiologies. Recent experimental studies reported an ...
Variação da acuidade visual em pacientes jovens com ectopia lentis submetidos à cirurgia
(Conselho Brasileiro de Oftalmologia, 2005-08-01)
PURPOSE: To assess the results as to visual acuity of two different surgical procedures for ectopia lentis. METHODS: Fifty-one eyes of 28 patients (16 males and 12 females, mean age 16.00± 8.5) with simple (19 cases) or ...