Ehlers-Danlos-Syndrom/en: Unterschied zwischen den Versionen
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Ehlers-Danlos syndrome (EDS) is a group of diseases characterized by an increased elasticity of the [[Haut/en|skin]]. The cause of some EDS species is probably a defective [[Kollagen/en|collagen]], the causes of other species are still unclear. | Ehlers-Danlos syndrome (EDS) is a group of diseases characterized by an increased elasticity of the [[Haut/en|skin]]. The cause of some EDS species is probably a defective [[Kollagen/en|collagen]], the causes of other species are still unclear. | ||
| − | In EDS there is a strong overstretching of the skin, [[Hämatom/en|haematoma]] inclination, over-mobility of the joints, spontaneous ruptures of [[ | + | 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/Loeys%E2%80%93Dietz_syndrome |
Aktuelle Version vom 14. März 2020, 09:05 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.