PedAM
Pediatric Disease Annotations & Medicines
| Disease | multiple system atrophy |
| Phenotype | C0007760|cerebellar disorders |
| Sentences | 1 |
| PubMedID- 26374734 | The studied patients were also carefully investigated to exclude other possible diagnoses including autoimmune cerebellar disorders, cerebellar variant of multiple system atrophy, and common mitochondrial dna mutations by using appropriated blood tests, genetic analysis of leukocyte, or muscle dna and neuroimaging. |
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