eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | muscular dystrophy |
| Comorbidity | C0023787|lipodystrophy |
| Sentences | 5 |
| PubMedID- 24375490 | Partial lipodystrophy associated with muscular dystrophy of unknown genetic origin. |
| PubMedID- 23489663 | Congenital generalized lipodystrophy type 4 with muscular dystrophy: clinical and pathological manifestations in early childhood. |
| PubMedID- 21119217 | In humans loss of ptrf-cavin also causes a secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy (42, 43). |
| PubMedID- 20447152 | Human ptrf mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy hayashi et al. |
| PubMedID- 24523287 | These include cardiomyopathy, lipodystrophy, and certain types of muscular dystrophy (mounkes et al., 2003; worman, 2012). |
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