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The diagnostic criteria for Classical EDS are primarily made up of skin and joint findings Bowen et al, There may be a family history of the condition but this is not always the case. Typical features of cEDS are: It is also hyper-elastic — it is stretched easily but it snaps back in to shape when released unlike certain skin conditions like Cutis Laxa, a condition associated with abnormality of the protein Elastin. Other skin findings that may appear in Classical EDS include:
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Classic Ehlers-Danlos syndrome Signs and symptoms of the most common form of Ehlers-Danlos syndrome include: Because the connective tissue that holds joints together is looser, your joints can move far past the normal range of motion. Joint pain and dislocations are common. Weakened connective tissue allows your skin to stretch much more than usual. You may be able to pull a pinch of skin up away from your flesh, but it will snap right back into place when you let go. Your skin might also feel exceptionally soft and velvety. Damaged skin often doesn't heal well.
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Ehlers–Danlos syndromes

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