Ehlers-Danlos Syndrome (EDS) is categorized into 13 distinct clinical types based on the affected tissues and the resulting symptoms. The most common types typically manifest with symptoms such as joint hypermobility (excessive flexibility) and fragile, easily torn skin. Vascular Ehlers-Danlos Syndrome (vEDS), on the other hand, is a more severe subtype affecting blood vessels and can lead to life-threatening complications.