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Ehlers Danlos syndrome is an inherited disorder and is characterized by the presence of extremely loose joints and stretched skins.
Some changes in genetic mutations can account for this disorder which impairs the functions of collagen. If the condition of the child is mild to moderate certain surgeries can be performed for correcting the heart functions.

The collagen is responsible for supporting strength to the skin, bone and blood vessels and when the functions are disturbed it will lead to the condition called hyper mobility (loose joints) and hyper-elasticity (loose skin) and weakened tissues. There are several types of ED syndrome disorder which differ with respect to the grouping of genetic material.
Wounds have to be treated with care and sutures can be difficult on the skin due to softness.

Unless there is sudden rupture of blood vessels the mortality rate of ED syndrome individuals are low.

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