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The John Ritter Research Program in Aortic and Vascular Diseases at the UT-Houston Medical School is working to prevent premature deaths due to thoracic aortic disease by improving diagnosis, treatment, and promote aortic health.
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GADA is focusing on: 1. Promoting the creation of multidisciplinary aortic (MDA) clinics, centres of excellence for the treatment of all genetic aortic disorders across Canada. 2. Expediting the development of diagnostic criteria and treatment protocols for each and every genetic aortic disorder. In order to achieve this objective, in 2013 GADA organized an intensive three-day inaugural meeting that took place in Italy which resulted in the creation of the Montalcino Aortic Consortium (MAC). Gene mutations have been identified to increase the risk of aortic aneurysms and dissections such as, mutations in the following genes: TGFBR1 & TGFBR2 – Loeys-Dietz syndrome FBN1 – Marfan syndrome, MYLK, ACTA2, SKI, TGFB2, SLC2A10, TGFB3 , MAT2A, SMAD(2/3/4), MFAP5, MYH11, PRKG1, FOXE3, LOX
Aortic Dissection Awareness – Increasing Aortic Awareness – Starting with YOU!.
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This is a 100% nonprofit page for the Global Aortic Disease Awareness Day September 19
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Find everything you need to know about Marfan syndrome including pictures of those affected by this genetic disease
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