Ehlers-Danlos syndrome (EDS) is not a single, homogeneous disorder, but a group of nine different types of genetically inherited disorders characterized by hyperelastic skin that is fragile and bruises easily, excessive laxity (looseness) of the joints, easily damaged blood vessels, and excessive bleeding. The syndrome is caused by abnormal formation of connective tissue due to mutations in collagen genes. Symptoms range from mild to severe within the six most prevalent types of the disorder.
Any of six inherited disorders of connective tissue (collagen and collagen-related proteins). Characteristic findings in most Ehler-Danlos patients include: joint hypermobility with dislocations (e.g., during childbirth) and velvety, loose and easily bruised skin. The syndrome is relatively rare. It affects about 1 child per 5000 births.
A rare genetic disorder affecting the connective tissue, characterized by extremely elastic skin, excessively flexible joints, and exceptionally fragile body tissues.
Ehlers-Danlos syndrome is a genetically transmitted condition that affects collagen, the body’s key structural protein. People living with this syndrome experience unusually elastic, delicate skin that is prone to bruising. They have wounds that heal slowly and leave behind thin scars, and they have hypermobile joints susceptible to repeated dislocations. They also tend to bleed easily, notably from the gums and digestive system.
Ehlers-Danlos syndrome is typically passed down through families following an autosomal dominant inheritance pattern. Currently, there isn’t a specific treatment available for this condition. However, those affected should take precautions to avoid unnecessary accidental injuries, like those that could potentially happen in contact sports.