2006
DOI: 10.2169/internalmedicine.45.1880
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Risk of Development of Abdominal Aortic Aneurysm and Dissection of Thoracic Aorta in a Postpartum Womanwith Marfans Syndrome

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Cited by 16 publications
(8 citation statements)
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“…The mean ± SD days after delivery for postpartum dissections in the MFS group ( n = 8) was 44 ± 78.50; in the non‐MFS group ( n = 13), these values were 11.23 ± 14.78, P = .280). The large standard deviation in the MFS group for postpartum dissections can be attributed to 2 outliers of dissections at 7‐months postpartum and 4‐months postpartum . The median values for days after delivery for presentation with a postpartum dissection were 5.5 days (range 1 day‐7 months) in the MFS group and 7 days (range 1 day‐2 months) in the non‐MFS group.…”
Section: Resultsmentioning
confidence: 96%
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“…The mean ± SD days after delivery for postpartum dissections in the MFS group ( n = 8) was 44 ± 78.50; in the non‐MFS group ( n = 13), these values were 11.23 ± 14.78, P = .280). The large standard deviation in the MFS group for postpartum dissections can be attributed to 2 outliers of dissections at 7‐months postpartum and 4‐months postpartum . The median values for days after delivery for presentation with a postpartum dissection were 5.5 days (range 1 day‐7 months) in the MFS group and 7 days (range 1 day‐2 months) in the non‐MFS group.…”
Section: Resultsmentioning
confidence: 96%
“…Only 6 of the MFS cases reported beta‐blocker therapy during the pregnancy . None of the cases with non‐MFS patients reported beta‐blocker therapy.…”
Section: Resultsmentioning
confidence: 99%
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“…M arfan syndrome is an autosomal dominant, multisystem disease characterized by long bone overgrowth and other skeletal abnormalities, such as dislocation of the ocular lens, pneumothorax, decreased skeletal muscle mass, mitral valve prolapse, and aortic arch dilatation. 1,2 The combination of structural microfibril matrix abnormalities, dysregulation of matrix homeostasis mediated by excess transforming growth factor, and abnormal cell-matrix interactions is responsible for the phenotypic features of Marfan syndrome. 1,3,4 Aortic dilatation in Marfan syndrome is related to degeneration of the medial layer, with fragmentation, disarray, and loss of elastic lamina with replacement by basophilic-staining proteoglycan.…”
mentioning
confidence: 99%