Le syndrome de Marfan est une maladie grave dont certaines complications peuvent être mortelles. Les progrès réalisés dans les soins médicaux permettent désormais aux personnes atteintes du syndrome de Marfan d’avoir une espérance de vie normale si elles reçoivent un diagnostic et un traitement adapté.
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Datos Sobre el Síndrome de Marfan
El Síndrome de Marfan es un trastorno del tejido conectivo. El tejido conectivo es el que hace que todas las partes del cuerpo se mantengan en su lugar y ayuda a controlar el crecimiento del cuerpo. Como el tejido conectivo se encuentra en todo el cuerpo, las características del Síndrome de Marfan pueden ocurrir en […]
Tags: Marfan Syndrome , Patients & Families
For families navigating life with a genetic aortic and vascular condition, the move from pediatric to adult care can feel like a mixed milestone. The transition often marks the first time a young person is expected to take primary responsibility for their health by managing appointments, medications, and decisions that were once made by parents/caregivers […]
Overview of Cardiac Management in Marfan Syndrome
Overview of Cardiac Management in Marfan Syndrome Aortic dissection is the major cause of premature morbidity and mortality in Marfan syndrome. Aortic root aneurysm or dissection and ectopia lentis are cardinal features of Marfan syndrome based on the 2010 Gent nosology. For the full diagnostic criteria, please visit MarfanDX.org. Cardiac features that may be seen […]
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