eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | leber hereditary optic neuropathy |
| Comorbidity | C0456909|vision loss |
| Sentences | 2 |
| PubMedID- 21788663 | Inclusion criteria were met if patients were between 14 and 64 years of age, harboured m.3460g>a, m.11778g>a, or m.14484t>c mitochondrial dna mutations, described vision loss due to lhon within 5 years, did not take drugs of abuse, and were neither pregnant nor breastfeeding. |
| PubMedID- 26170609 | Although lhon usually presents with isolated vision loss, some patients suffer other neurological sequelae. |
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