eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | muscular atrophy |
| Comorbidity | C0030486|paraplegia |
| Sentences | 3 |
| PubMedID- 25731823 | They were also absent from cohorts of spinal muscular atrophy and patients with hereditary spastic paraplegia [45–47]. |
| PubMedID- 20039086 | These findings indicate a clinically and genetically distinct form of hereditary spastic paraplegia with amyotrophy, designated spg43. |
| PubMedID- 23055316 | Conclusions: severe muscle atrophy resulting from chronic paraplegia appears to increase skeletal muscle autophagy independent of sirt1 signaling. |
Page: 1