Hypermobile Ehlers-Danlos is one of six different types of Ehlers-Danlos syndromes, and it is the most common. Hypermobile Ehlers-Danlos is a connective tissue disorder that predominantly affects the skeletal system. It is characterized by loose joints, often associated with chronic (long-term) joint pain.
What other names do people use for Hypermobile Ehlers-Danlos?
What are the characteristics of Hypermobile Ehlers-Danlos?
What causes Hypermobile Ehlers-Danlos?
How is Hypermobile Ehlers-Danlos managed?
Find these answers and more in the “Hypermobile Ehlers-Danlos” download.
Molte persone affette da sindrome di Marfan o alcune malattie correlate hanno una mascella stretta e un palato alto e arcuato, che possono causare problemi dentali e ortodontici. Inoltre, chi presenta prolasso della valvola mitrale ed è portatore di valvole cardiache artificiali è a rischio di endocardite (infezione del cuore e delle valvole cardiache) in […]
A concise, evidence-based clinical guidance document from the Marfan Foundation in collaboration with Luciana Young, MD, offering families, pediatricians, and cardiologists practical information on evaluating and treating ADHD in children with genetic aortic and vascular conditions such as Marfan syndrome, Loeys-Dietz syndrome, and Vascular Ehlers-Danlos syndrome. This article is intended for educational purposes only and […]
Les personnes atteintes du syndrome de Marfan présentent souvent des problèmes au niveau du coeur et des vaisseaux sanguins. Ces problèmes peuvent parfois être très graves. La complication la plus fréquente concerne l’aorte (le principal vaisseau sanguin qui transporte le sang du coeur vers le reste du corps). Les valves cardiaques peuvent également être affectées. […]
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