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Dimensions of Critical Care Nursing, 2000
Cardiac complications of Marfan syndrome can be fatal. This article reviews the assessment of a patient with this hereditary disorder, complications and their treatment, and nursing care.
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Cardiac complications of Marfan syndrome can be fatal. This article reviews the assessment of a patient with this hereditary disorder, complications and their treatment, and nursing care.
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Schizophrenia and Marfan Syndrome
British Journal of Psychiatry, 1990Five index patients and three of their first-degree relatives were affected both by schizophrenia and Marfan syndrome. Since the association appears statistically significant, the possibility of linkage disequilibrium between adjacent genes or a cytogenetic abnormality causing both disorders is suggested.
P, Sirota, M, Frydman, L, Sirota
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AORN Journal, 1986
Marfan's patients share the same problems as anyone with a lifelong, progressive, hereditary condition. The more knowledgeable an individual is about his disease and the more willing he is to accept the responsibility for his own well-being, the more control he has over his life. Medical and life insurance is not a luxury, but an absolute must.
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Marfan's patients share the same problems as anyone with a lifelong, progressive, hereditary condition. The more knowledgeable an individual is about his disease and the more willing he is to accept the responsibility for his own well-being, the more control he has over his life. Medical and life insurance is not a luxury, but an absolute must.
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Nursing
Abstract: This article provides a comprehensive review of Marfan Syndrome (MFS), covering its epidemiology, etiology, clinical presentations, diagnostics, complications, and treatment modalities. The Ghent II Nosology of MFS criteria are crucial in MFS diagnosis, guiding clinicians in identifying high-risk patients.
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Abstract: This article provides a comprehensive review of Marfan Syndrome (MFS), covering its epidemiology, etiology, clinical presentations, diagnostics, complications, and treatment modalities. The Ghent II Nosology of MFS criteria are crucial in MFS diagnosis, guiding clinicians in identifying high-risk patients.
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Coarctation in the Marfan Syndrome
Archives of Internal Medicine, 1964The Marfan syndrome is now recognized as a heritable disorder of connective tissue that usually follows a simple mendelian dominant pattern of Transmission. 1 Manifestations of the abnormality are quite variable but are seen most often in the cardiovascular, musculoskeletal, and ocular systems. Coarctation of the aorta is not one of the common findings
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