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Ehlers-Danlos’ syndrom

Klinisk undersøgelse af hudens overtrækbarhed testes på volarsiden af underarmen.
Forfatter(e)
Julie Leganger1, Marie-Louise Kulas Søborg1, Stense Farholt2, Allan Meldgaard Lund3, Jacob Rosenberg1 & Jakob Burcharth1 1) Center for Perioperativ Optimering (CPO), Gastroenheden, Kirurgisk Sektion, Herlev Hospital2) Center for Sjældne Sygdomme, Aarhus Universitetshospital 3) Center for Sjældne Sygdomme, Rigshospitalet Ugeskr Læger 2016:178:V01160014
Reference: 
Ugeskr Læger 2016:178:V01160014
Blad nummer: 
Sidetal: 
2
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome (EDS) comprises a group of diseases characterized by connective tissue fragility. The clinical symptoms primarily involve the skin, joints, blood vessels and internal organs. Diagnosing EDS is complicated because of the clinical variability, imprecise diagnostic criteria, and because physicians may lack knowledge of this rare disease. The aim of this article is to provide an overview of the clinical symptoms and to provide recommendations on diagnosis and treatment. Referring patients to one of the national centres for rare diseases is important.
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