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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 [[skin]]. The cause of some EDS species is probably a defective [[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 [[skin]]. The cause of some EDS species is probably a defective [[collagen]], the causes of other species are still unclear.  
  
Beim EDS zeigen sich eine stark überdehnbare Haut, [[Hämatom]]-Neigung, Überbeweglichkeit der Gelenke, spontane Rupturen von [[Arterie]]n und Gefäßen. EDS gehört mit einem Auftreten von 1:5.000 bis ca. 1:10.000 zu den seltenen Krankheiten.
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In EDS there is a strong overstretching of the skin, [[haematoma]] inclination, over-mobility of the joints, spontaneous ruptures of [[artery]] and vessels. EDS is a rare disease with an incidence of 1:5,000 to approx. 1:10,000.
  
 
https://de.wikipedia.org/wiki/Ehlers-Danlos-Syndrom <sub>([http://de.wikipedia.org/wiki/Wikipedia:Lizenzbestimmungen_Commons_Attribution-ShareAlike_3.0_Unported Wikipedia CC-by-sa-3.0])</sub>
 
https://de.wikipedia.org/wiki/Ehlers-Danlos-Syndrom <sub>([http://de.wikipedia.org/wiki/Wikipedia:Lizenzbestimmungen_Commons_Attribution-ShareAlike_3.0_Unported Wikipedia CC-by-sa-3.0])</sub>

Version vom 16. April 2019, 21:32 Uhr

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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 artery and vessels. EDS is a rare disease with an incidence of 1:5,000 to approx. 1:10,000.

https://de.wikipedia.org/wiki/Ehlers-Danlos-Syndrom (Wikipedia CC-by-sa-3.0)