eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | neurofibromatosis |
| Symptom | C0017601|glaucoma |
| Sentences | 6 |
| PubMedID- 26514695 | A rare case of primary congenital glaucoma in combination with neurofibromatosis 1: a case report. |
| PubMedID- 22138687 | Iris neovascularization and neovascular glaucoma in neurofibromatosis type 1: report of 3 cases in children. |
| PubMedID- 25762928 | Unusual case of angle closure glaucoma in a patient with neurofibromatosis type 1. |
| PubMedID- 19340401 | Management of congenital glaucoma in neurofibromatosis type 1: a report of two cases. |
| PubMedID- 21766740 | The authors present the diagnostic challenge of an unusual case of neurofibromatosis type 1 with unilateral congenital glaucoma, buphthalmos, and sphenoid-orbital dysplasia. |
| PubMedID- 22480745 | Congenital ectropion uvea and mechanisms of glaucoma in neurofibromatosis type 1: new insights. |
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