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As individuals with Ehlers-Danlos Syndrome age, they may experience several changes that can affect their quality of life. Joint stability often decreases, and there is an increased risk of developing osteoarthritis, particularly in the knees, hips, and hands. Skin elasticity and healing capacity may diminish, leading to more pronounced scarring and bruising. Cardiovascular issues, such as varicose veins and an increased risk of heart valve problems, may also become more apparent.
Life expectancy in individuals with EDS varies depending on the type and severity of the disorder. Most types of EDS do not significantly affect life expectancy, but some complications associated with vascular EDS, such as organ and vessel rupture, can be life-threatening. Regular medical reviews and proactive management of symptoms are essential. For more detailed information on the impact of EDS on life expectancy, refer to the comprehensive studies and guidelines available at NIH’s Genetics Home Reference.
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