Publication: Cardiomyopathy in duchenne muscular dystrophy: current value of clinical, electrophysiological and imaging findings in children and teenagers
Cardiomyopathy in duchenne muscular dystrophy: current value of clinical, electrophysiological and imaging findings in children and teenagers
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Dittrich, S., Tuerk, M., Haaker, G., Greim, V., Buchholz, A., Burkhardt, B., Fujak, A., Trollmann, R., Schmid, A., & Schroeder, R. (2015). Cardiomyopathy in duchenne muscular dystrophy: current value of clinical, electrophysiological and imaging findings in children and teenagers. Klinische Pädiatrie, 227(4), 225–231. https://doi.org/10.1055/s-0034-1398689
Abstract
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Abstract
BACKGROUND: Progressive cardiomyopathy (CMP) is one main cause of death in DMD. This cross-sectional assessment of different cardiac diagnostic procedures focusses on preterm diagnosis of cardiac dysfunction. PATIENTS: 39 male DMD patients aged 6-20 years were included. 6 patients were still ambulatory, 21 patients received corticosteroid therapy. METHODS: All patients were investigated by ECG, Holter ECG and heart rate variability (HRV), B-type natriuretic peptide (BNP), echocardiography (TTE), tissue Doppler Imaging (TD) and magneti
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Creators (Authors)
- Dittrich, S
- Tuerk, M
- Haaker, G
- Greim, V
- Buchholz, A
- Burkhardt, B
- Fujak, A
- Trollmann, R
- Schmid, A
- Schroeder, R
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Citations
Dittrich, S., Tuerk, M., Haaker, G., Greim, V., Buchholz, A., Burkhardt, B., Fujak, A., Trollmann, R., Schmid, A., & Schroeder, R. (2015). Cardiomyopathy in duchenne muscular dystrophy: current value of clinical, electrophysiological and imaging findings in children and teenagers. Klinische Pädiatrie, 227(4), 225–231. https://doi.org/10.1055/s-0034-1398689
