Ehlers-Danlos-Syndrom/en: Unterschied zwischen den Versionen
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In EDS there is a strong overstretching of the skin, [[Hämatom/en|haematoma]] inclination, over-mobility of the joints, spontaneous ruptures of [[Aorta/en|aorta]] and other vessels. EDS is a rare disease with an incidence of 1:5,000 to approx. 1:10,000. | In EDS there is a strong overstretching of the skin, [[Hämatom/en|haematoma]] inclination, over-mobility of the joints, spontaneous ruptures of [[Aorta/en|aorta]] and other vessels. EDS is a rare disease with an incidence of 1:5,000 to approx. 1:10,000. | ||
| − | https:// | + | https://en.wikipedia.org/wiki/Ehlers%E2%80%93Danlos_syndromes <sub>([https://en.wikipedia.org/wiki/Wikipedia:Text_of_Creative_Commons_Attribution-ShareAlike_3.0_Unported_License])</sub> |
Version vom 20. Juli 2019, 13:33 Uhr
Ehlers-Danlos syndrome (EDS) is a group of diseases characterized by an increased elasticity of the skin. The cause of some EDS species is probably a defective collagen, the causes of other species are still unclear.
In EDS there is a strong overstretching of the skin, haematoma inclination, over-mobility of the joints, spontaneous ruptures of aorta and other vessels. EDS is a rare disease with an incidence of 1:5,000 to approx. 1:10,000.
https://en.wikipedia.org/wiki/Ehlers%E2%80%93Danlos_syndromes ([1])