SciELO - Scientific Electronic Library Online

 
vol.10 issue1Endometriosis implants after cesarean section: more than a scar - a case report author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Acta Obstétrica e Ginecológica Portuguesa

Print version ISSN 1646-5830

Abstract

AMARAL, Patrícia Isidro; CAMPOS, Ana  and  PATRICIO, Lino. Pregnancy in Marfan Syndrome: two case reports. Acta Obstet Ginecol Port [online]. 2016, vol.10, n.1, pp.74-77. ISSN 1646-5830.

Marfan syndrome is a connective tissue disorder, autosomal dominant, which affects multiple organ systems, namely the cardiovascular, ocular and skeletal. Morbidity and mortality result primarily from aortic and cardiac complications including dilatation, dissection and rupture of the aorta. As a result, pregnancy in women with the Marfan syndrome has an increased risk. Main causes of complications are related with hemodynamic and hormonal modifications caused by pregnancy. The approach to pregnancy in patients with this syndrome is challenging and deserves special care. A multidisciplinary surveillance plan should be developed with support from cardiology, maternal fetal medicine, anesthesiology, genetics and pediatrics.

Keywords : Marfan Syndrome; Pregnancy; Aortic dilatation.

        · text in Portuguese     · Portuguese ( pdf )