La dilatación de la raíz de la aorta es cuando el segmento de la aorta más cercano al corazón se encuentra agrandado. Este es un problema muy serio y muy común para personas con síndrome de Marfan. Con frecuencia el tratamiento para cuando la raíz aortica alcanza cierto tamaño es una cirugía; si la raíz aortica se desgarra (disección aortica), se requiere de cirugía de emergencia.
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Planification Familiale Et Grossesse
Les décisions relatives à la planification familiale peuvent être difficiles et susciter beaucoup d’émotions lorsque l’un des parents potentiels est atteint d’une maladie génétique, comme le syndrome de Marfan. Avant toute décision, les parents doivent connaître les nombreuses options actuellement disponibles ainsi que les risques encourus par l’enfant et la mère. Un conseiller en génétique […]
Tags: Marfan Syndrome , Patients & Families
COVID-19 Vaccine Statements
The Foundation’s Professional Advisory Board has issued an updated 2025 statement regarding COVID-19 vaccinations for both adults and children with Marfan, Loeys-Dietz, and VEDS, and related conditions. This guidance reflects the latest research and clinical expertise to help individuals and families make informed decisions about vaccination and ongoing health protection. If you have additional medical […]
Heart and Blood Vessels
People with Marfan syndrome frequently have problems with their heart and blood vessels. Sometimes, these problems are very serious. The most common complication affects the aorta (the main blood vessel carrying blood from the heart to the rest of the body). Heart valves may be affected as well. Less often, blood vessels other than the […]
Tags: Marfan Syndrome , Patients & Families
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