All types of EDS affect the joints, and most also affect the skin. At Mayo Clinic, teams of experienced and highly trained specialists work with patients to identify the most appropriate treatment for each type of EDS.
Ehlers-Danlos syndrome is classified according to the signs and symptoms exhibited by patients.
Congenital hip dislocation
Severe joint hypermobility (extreme flexibility)
Skin hyperextensibility (extreme stretchiness)
Frail skin tissue
Skin hyperextensibility
Joint hypermobility
Smooth, velvety skin
Widened scars over pressure points such as knees
Severe skin fragility
Soft, doughy and saggy skin
Joint hypermobility
Joint dislocations
Chronic joint and limb pain
Smooth, velvety skin
Joint laxity and weak muscle tone at birth
Delayed gross motor development
Progressive, severe symptoms
Possibility of spontaneous arterial rupture
Ruptures of the arteries, organs or uterus
Thin, translucent skin over the chest and abdomen
Extensive bruising
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