Ehlers-Danlos' syndrom

Julie Leganger; Marie-Louise Kulas Søborg; Stense Farholt; Allan Meldgaard Lund; Jacob Rosenberg; Jakob Burcharth

Ehlers-Danlos' syndrom

Julie Leganger, Marie-Louise Kulas Søborg, Stense Farholt, Allan Meldgaard Lund, Jacob Rosenberg, Jakob Burcharth

Institut for Klinisk Medicin

2 Citationer (Scopus)

Abstract

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.

Bidragets oversatte titel	Ehlers-Danlos syndrome
Originalsprog	Dansk
Artikelnummer	V01160014
Tidsskrift	Ugeskrift for Laeger
Vol/bind	178
Udgave nummer	17
Sider (fra-til)	2
Antal sider	1
ISSN	0041-5782
Status	Udgivet - 25 apr. 2016

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http://ugeskriftet.dk/videnskab/ehlers-danlos-syndromLicens: Ikke-specificeret

Citationsformater

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abstract = "Ehlers-Danlos syndromeEhlers-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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T1 - Ehlers-Danlos' syndrom

AU - Leganger, Julie

AU - Søborg, Marie-Louise Kulas

AU - Farholt, Stense

AU - Lund, Allan Meldgaard

AU - Rosenberg, Jacob

AU - Burcharth, Jakob

PY - 2016/4/25

Y1 - 2016/4/25

N2 - Ehlers-Danlos syndromeEhlers-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.

AB - Ehlers-Danlos syndromeEhlers-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.

KW - English Abstract

KW - Journal Article

M3 - Tidsskriftartikel

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SN - 0041-5782

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JO - Ugeskrift for Laeger

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Ehlers-Danlos' syndrom

Abstract

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