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Marfan's syndrome and surgical repair of ascending aortic aneurysms.
Wieczorek, P; Riegel, M B; Quattro, L; DeMaio, K.
Afiliação
  • Wieczorek P; Johns Hopkins Hospital, Baltimore, USA.
AORN J ; 64(6): 895-913; quiz 916-8, 921-2, 1996 Dec.
Article em En | MEDLINE | ID: mdl-8960679
ABSTRACT
Marfan's syndrome is an inherited, degenerative connective tissue disorder that affects many body systems (eg, skeletal, ocular, cardiovascular, cutaneous, pulmonary, abdominal, neurologic). The cause of Marfan's syndrome is unknown, but recent genetic studies have linked this disorder to chromosome 15q15-q21.3. The characteristics associated with Marfan's syndrome require a multidisciplinary approach to patient care. This article discusses one serious complication of Marfan's syndrome-aortic root dilatation- and composite graft repairs of ascending aortic aneurysms. Physicians and nurses must be more aware of Marfan's syndrome so that life-threatening medical conditions can be evaluated and followed by health care providers.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Aórtico / Enfermagem Perioperatória / Próteses Valvulares Cardíacas / Síndrome de Marfan Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 1996 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Aórtico / Enfermagem Perioperatória / Próteses Valvulares Cardíacas / Síndrome de Marfan Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 1996 Tipo de documento: Article