PedAM
Pediatric Disease Annotations & Medicines
| Disease | muscular dystrophy |
| Symptom | C0007193|dilated cardiomyopathy |
| Sentences | 14 |
| PubMedID- 21596026 | Circulating tenascin-c levels in patients with dilated cardiomyopathy in the course of emery-dreifuss muscular dystrophy. |
| PubMedID- 20182615 | These diseases include dilated cardiomyopathy with variable muscular dystrophy, dunnigan-type familial partial lipodystrophy, a charcot-marie-tooth type 2 disease, mandibuloacral dysplasia, and hutchinson-gilford progeria syndrome. |
| PubMedID- 24996370 | A novel dystrophin deletion mutation in a becker muscular dystrophy patient with early-onset dilated cardiomyopathy. |
| PubMedID- 26050665 | At the age of 23, he was admitted to the hospital for severe dilated cardiomyopathy, and subsequently diagnosed with limb-girdle muscular dystrophy2m (lgmd2m) based on muscle biopsy and gene analysis. |
| PubMedID- 23933734 | Mutations in the lamin a/c gene (lmna) encoding a-type nuclear lamins cause dilated cardiomyopathy with variable muscular dystrophy. |
| PubMedID- 23048029 | Mutations in the lamin a/c gene (lmna) cause a diverse spectrum of diseases, the most common of which is dilated cardiomyopathy often with skeletal muscular dystrophy. |
| PubMedID- 22077867 | Osteopontin--a fibrosis-related marker--in dilated cardiomyopathy in patients with emery-dreifuss muscular dystrophy. |
| PubMedID- 22655514 | However carvedilol therapy can be safe for patients with dilated cardiomyopathy associated with muscular dystrophy, even producing a modest improvement in systolic and diastolic function (26). |
| PubMedID- 23400933 | A dilated cardiomyopathy (dcm) is associated with duchenne muscular dystrophy (dmd). |
| PubMedID- 23418438 | The homozygous mice develop, similarly to human patients, progressive muscular dystrophy associated with dilated cardiomyopathy . |
| PubMedID- 20501885 | The duchenne and becker forms of muscular dystrophy are associated with dilated cardiomyopathy and are diseases in which pulmonary function peaks and then progressively declines. |
| PubMedID- 20497525 | Kuru et al3 reported a 57-year-old japanese woman with dysferlinopathy manifested as secondary dilated cardiomyopathy attributable to muscular dystrophy. |
| PubMedID- 25563468 | Hitherto, they have not been examined in dilated cardiomyopathy in the course of emery-dreifuss muscular dystrophy (edmd). |
| PubMedID- 25996830 | These findings suggest that reductive stress might contribute to the dilated cardiomyopathy in cases of lamin associated muscular dystrophy. |
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