Persa, O. D., Moinzadeh, P. and Hunzelmann, N. (2015). Systemic sclerosis. Current classification and diagnosis of organ involvement. Hautarzt, 66 (8). S. 599 - 604. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1432-1173

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Abstract

Systemic sclerosis (SSc) is a rare, chronic inflammatory autoimmune disease with unknown etiology, which leads to deposition of collagen and extracellular matrix proteins in the skin and affected internal organs. The diagnosis of SSc is based on clinical, serological, and paraclinical examinations. In 2013 new criteria for the classification of systemic sclerosis, which also take early forms of SSc into consideration, were developed. A complete clinical and paraclinical examination is important for the oligosymptomatic early stages and the subsequent disease course of SSc in order to diagnose and timely treat a developing organ involvement.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Persa, O. D.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Moinzadeh, P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hunzelmann, N.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-397554
DOI: 10.1007/s00105-015-3653-6
Journal or Publication Title: Hautarzt
Volume: 66
Number: 8
Page Range: S. 599 - 604
Date: 2015
Publisher: SPRINGER HEIDELBERG
Place of Publication: HEIDELBERG
ISSN: 1432-1173
Language: German
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
GERMAN NETWORK; SCLERODERMA; DISEASE; AUTOANTIBODIES; PROGRESSION; FREQUENCY; CRITERIA; SUBSETS; DEATHMultiple languages
DermatologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/39755

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