AB0883 IDIOPATHIC OPHTHALMIC MYOSITIS: CLINICAL PRESENTATION, THERAPEUTIC APPROACH AND IMAGING DIFFE...
AB0883 IDIOPATHIC OPHTHALMIC MYOSITIS: CLINICAL PRESENTATION, THERAPEUTIC APPROACH AND IMAGING DIFFERENTIATION FROM GRAVES OPHTHALMOPATHY
About this item
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Publisher
Kidlington: Elsevier B.V
Journal title
Language
English
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Publisher
Kidlington: Elsevier B.V
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Scope and Contents
Contents
Idiopathic ophthalmic myositis (IOM) represents a rare autoimmune ophthalmoplegia of unknown etiology, that may mimic predominantly Graves' ophthalmopathy (GO). IOM is characterized by pronounced inflammatory infiltration of extraocular muscles leading to fibrosis and eye-threatening complications, if remains untreated [1,2]. The rarity and clinica...
Alternative Titles
Full title
AB0883 IDIOPATHIC OPHTHALMIC MYOSITIS: CLINICAL PRESENTATION, THERAPEUTIC APPROACH AND IMAGING DIFFERENTIATION FROM GRAVES OPHTHALMOPATHY
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TN_cdi_proquest_journals_2854318590
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2854318590
Other Identifiers
ISSN
0003-4967
E-ISSN
1468-2060
DOI
10.1136/annrheumdis-2023-eular.4734
