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Updated: Jul 17, 2026

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
[Central core myopathy: a juvenile and adult disease]
H J Gdynia1, A-D Sperfeld, C O Hanemann
1Muskellabor der Neurologischen Universitätsklinik Ulm, Oberer Eselsberg 45, 89081 Ulm, Deutschland. hans-juergen.gdynia@uni-ulm.de
Abstract:
Central core myopathy is a nonprogressive or only slowly progressive congenital muscle disease. In most cases, symptoms begin in childhood, but rare cases with adult onset are described. Regardless of its high variability, the clinical hallmarks are diffuse muscle weakness and the development of multiple bone deformities and contractures. Skeletal muscle biopsy is of high diagnostic significance. Due to a potential association with malignant hyperthermia, early diagnosis is of great importance. A curative treatment is not currently known. Here we discuss aetiology, pathogenesis, clinical features, diagnosis, differential diagnosis, therapeutic strategies, and prognosis of central core myopathy based on a clinical example with an atypical onset of symptoms in adulthood.
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