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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://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>
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https://en.wikipedia.org/wiki/Loeys%E2%80%93Dietz_syndrome

Aktuelle Version vom 14. März 2020, 09:05 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 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/Loeys%E2%80%93Dietz_syndrome