Publication:
Eosinophilic myositis as presenting symptom in γ-sarcoglycanopathy

dc.contributor.authorBaumeister, Sarah K. (59048966100)
dc.contributor.authorTodorovic, Slobodanka (7005263658)
dc.contributor.authorMilić-Rašić, Vedrana (6507653181)
dc.contributor.authorDekomien, Gabriele (6603417157)
dc.contributor.authorLochmüller, Hanns (7005290364)
dc.contributor.authorWalter, Maggie C. (7402841766)
dc.date.accessioned2025-07-02T12:45:33Z
dc.date.available2025-07-02T12:45:33Z
dc.date.issued2009
dc.description.abstractThe patient reported here presented with first symptoms at the age of 10 showing an abnormal gait, calf hypertrophy and winged scapulae. She was diagnosed with eosinophilic myositis after muscle biopsy. A second muscle biopsy at the age of 20 and subsequent genetic testing, however, revealed the underlying condition of a primary γ-sarcoglycanopathy, or LGMD2C. To our knowledge, this is the first LGMD2C patient reported who initially presented with eosinophilic myositis. Eosinophilia has been reported previously in patients with Calpainopathy and Becker Muscular Dystrophy and might be an early, but transient feature of a wider range of muscular dystrophies. © 2008 Elsevier B.V. All rights reserved.
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2008.11.010
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-59249092358&doi=10.1016%2fj.nmd.2008.11.010&partnerID=40&md5=5346ae86635081a558ead8cbda5ce1f4
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/14171
dc.subjectγ-Sarcoglycanopathy
dc.subjectEosinophilic myositis
dc.subjectLGMD2C
dc.subjectLimb girdle muscular dystrophy
dc.titleEosinophilic myositis as presenting symptom in γ-sarcoglycanopathy
dspace.entity.typePublication

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