Atıf İçin Kopyala
Oflazer P. S., Gundesli H., ZORLUDEMİR S., Sabuncu T., Dincer P.
NEUROMUSCULAR DISORDERS, cilt.19, sa.4, ss.261-263, 2009 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
19
Sayı:
4
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Basım Tarihi:
2009
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Doi Numarası:
10.1016/j.nmd.2009.01.010
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Dergi Adı:
NEUROMUSCULAR DISORDERS
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.261-263
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Anahtar Kelimeler:
Calpainopathy, LGMD 2A, Eosinophilic myositis, Muscular dystrophy, MUSCULAR-DYSTROPHY, CAPN3 MUTATIONS, INFLAMMATION, CALPAIN-3, PROTEIN, MUSCLE, DYSFERLIN
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Hacettepe Üniversitesi Adresli:
Evet
Özet
An 11-year-old girl with a calpain-3 gene (CAPN-3) mutation and eosinophilic myositis on muscle biopsy had high serum CK levels and eosinophil counts which showed spontaneous fluctuations. After commencement of immunosuppressive therapy reciprocal changes occured in response to alterations in closes of the medications. Subacutely evolving and spreading muscle weakness developed during tapering of the immunosuppressive medications.