Results 271 to 280 of about 2,218,154 (303)
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2023
Abstract: Marfan syndrome (MFS) is an autosomal dominant disorder of connective tissue, involving the cardiovascular, ocular, and skeletal systems, as well as the lungs, dura, and skin. Cardiovascular complications, including aortic root dilatation, aortic dissection and rupture, mitral valve prolapse, mitral and/or aortic valve regurgitation, begin in
Vanhoenacker, Filip +2 more
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Abstract: Marfan syndrome (MFS) is an autosomal dominant disorder of connective tissue, involving the cardiovascular, ocular, and skeletal systems, as well as the lungs, dura, and skin. Cardiovascular complications, including aortic root dilatation, aortic dissection and rupture, mitral valve prolapse, mitral and/or aortic valve regurgitation, begin in
Vanhoenacker, Filip +2 more
openaire +4 more sources
Perinatal diagnosis and management of early-onset Marfan syndrome: case report and systematic review
Journal of Maternal-Fetal & Neonatal Medicine, 2020Early onset Marfan syndrome is the most severe form of Marfan syndrome diagnosed during perinatal period. Early onset Marfan syndrome is associated with high mortality rates, usually within the first 2 years of life.
A. Veiga-Fernández +8 more
semanticscholar +1 more source
Trends of vascular surgery procedures in Marfan syndrome and Ehlers-Danlos syndrome
Vascular, 2020Objectives Marfan syndrome and Ehlers-Danlos syndrome represent two connective tissue vascular diseases requiring unique consideration in their vascular surgical care.
S. Jayarajan +3 more
semanticscholar +1 more source
Annals of Emergency Medicine, 1980
Asfaw I, Tintinalli JE: Marfan's syndrome. Ann Emerg Med 9:105-107, February 1 980. Marfan's syndrome; syndrome, Marfan's; aortic insufficiency, Marfan's syndro me I NTRODUCTION Judith Tintinalli, MD: The case for discussion today is that of a young woman with Marfan's syndrome and chest pain.
Judith E. Tintinalli, Ingida Asfaw
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Asfaw I, Tintinalli JE: Marfan's syndrome. Ann Emerg Med 9:105-107, February 1 980. Marfan's syndrome; syndrome, Marfan's; aortic insufficiency, Marfan's syndro me I NTRODUCTION Judith Tintinalli, MD: The case for discussion today is that of a young woman with Marfan's syndrome and chest pain.
Judith E. Tintinalli, Ingida Asfaw
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European Heart Journal, 2019
AIMS Life expectancy in Marfan syndrome patients has improved thanks to the early detection of aortic dilation and prophylactic aortic root surgery.
A. Guala +13 more
semanticscholar +1 more source
AIMS Life expectancy in Marfan syndrome patients has improved thanks to the early detection of aortic dilation and prophylactic aortic root surgery.
A. Guala +13 more
semanticscholar +1 more source
JAMA cardiology, 2019
Importance Thoracic aortic aneurysms leading to acute aortic dissections are a major cause of morbidity and mortality despite significant advances in surgical treatment, which remains the main intervention to prevent type A dissections.
Marion A. Hofmann Bowman +2 more
semanticscholar +1 more source
Importance Thoracic aortic aneurysms leading to acute aortic dissections are a major cause of morbidity and mortality despite significant advances in surgical treatment, which remains the main intervention to prevent type A dissections.
Marion A. Hofmann Bowman +2 more
semanticscholar +1 more source
Journal of the American Academy of Nurse Practitioners, 2009
AbstractPurpose: To provide an overview of Marfan syndrome (MFS), including diagnostic criteria, genetic factors involved, emerging theories for treatment, a case study, and an overview of genetic counseling for individuals and families of those with MFS.Data Sources: Selected research, review, and clinical articles.Conclusions: MFS is a connective ...
Eric D, Shirley, Paul D, Sponseller
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AbstractPurpose: To provide an overview of Marfan syndrome (MFS), including diagnostic criteria, genetic factors involved, emerging theories for treatment, a case study, and an overview of genetic counseling for individuals and families of those with MFS.Data Sources: Selected research, review, and clinical articles.Conclusions: MFS is a connective ...
Eric D, Shirley, Paul D, Sponseller
openaire +4 more sources
Marfan's syndrome or the Marfan syndrome
International Journal of Cardiology, 1987The eponym of the well-characterised clinical syndrome has peculiarly been accepted both as Marfan’s syndrome and as the Marfan syndrome. Amongst the five major textbooks of internal medicine and cardiology. two have used Marfan’s syndrome (I.21 and three the Marfan syndrome [3-51. Thirty years ago McKusick wrote “Marfan’s Syndrome or better the Marfan
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American Heart Journal, 1953
Abstract A case of Marfan's syndrome exhibiting medial degeneration and aneurysmal formation with incomplete rupture of the pulmonary artery is reported with a review of the literature.
H.R. Pratt-Thomas, Maxwell Anderson
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Abstract A case of Marfan's syndrome exhibiting medial degeneration and aneurysmal formation with incomplete rupture of the pulmonary artery is reported with a review of the literature.
H.R. Pratt-Thomas, Maxwell Anderson
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Annual Review of Medicine, 2000
▪ Abstract The Marfan syndrome (MFS), initially described just over 100 years ago, was among the first conditions classified as a heritable disorder of connective tissue. MFS lies at one end of a phenotypic continuum, with people in the general population who have one or another of the features of MFS at the other end, and those with a variety of ...
openaire +4 more sources
▪ Abstract The Marfan syndrome (MFS), initially described just over 100 years ago, was among the first conditions classified as a heritable disorder of connective tissue. MFS lies at one end of a phenotypic continuum, with people in the general population who have one or another of the features of MFS at the other end, and those with a variety of ...
openaire +4 more sources