DSpace Repository

A Rare Clinical Condition: Erasmus Syndrome

Show simple item record

dc.creator DOĞRU, Atalay
dc.creator Tunc, Sevket Ercan
dc.creator Ugan, Yunus
dc.creator ŞAHİN, Mehmet
dc.date 2016-06-30T21:00:00Z
dc.date.accessioned 2020-10-06T09:32:34Z
dc.date.available 2020-10-06T09:32:34Z
dc.identifier 23c00cd8-7b37-45c0-8f32-c967c69192fe
dc.identifier 10.4328/jcam.4271
dc.identifier https://avesis.sdu.edu.tr/publication/details/23c00cd8-7b37-45c0-8f32-c967c69192fe/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/55456
dc.description Systemic sclerosis (SS) is a systemic autoimmune disease progressing with fibrosis of the skin and internal organs, the cause of which cannot be precisely explained. The disease is known to be associated with environmental factors. In particular, exposure to silica powders is believed to have a part in the pathogenesis of the disease by the triggering of a number of immune reactions. Silicosis and SS association is defined as Erasmus Syndrome (ES). Here, we report on a 30-year-old patient working in denim sandblasting who developed SS while being followed for 6 years due to silicosis.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title A Rare Clinical Condition: Erasmus Syndrome
dc.type info:eu-repo/semantics/article

Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search DSpace

Advanced Search


My Account