eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | papilledema |
| Comorbidity | C0010278|craniosynostosis |
| Sentences | 2 |
| PubMedID- 22220162 | Methods: case report of a 3-year-old female presenting with papilledema resulting from craniosynostosis secondary to xlh. |
| PubMedID- 24519451 | Given the quantitative character, oct has a high potential as an alternative tool to screen for papilledema in craniosynostosis and other pediatric populations. |
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